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Symptom Checker » Epilepsy » Gait ataxia
 

Epilepsy and Gait ataxia
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Results: Causes of Epilepsy AND Gait ataxia

    1. Spinocerebellar ataxia 13
     A rare genetic disorder (chromosome 19 defect) characterized by progressive mental retardation. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....read more »

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Results: 168 causes of Epilepsy OR Gait ataxia

    1. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    2. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    3. Alveolar Hydatid Disease
     Rare multi-organ tapeworm infection caught from animals....more »
    4. Amelo-cerebro-hypohidrotic syndrome
     A rare syndrome involving degeneration of the central nervous system, seizures and abnormal tooth development....more »
    5. Angelman syndrome
     A rare genetic disorder characterized by a puppet-like gait, fits of laughter and characteristic facial features....more »
    6. Angelman-Like Syndrome, X-linked
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    7. Anophthalmia -- hypothalamo-pituitary insufficiency
     A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland....more »
    8. Anophthalmia -- hypyothalamo-pituitary insufficiency
     A rare syndrome characterized mainly by small or absent eyes and malformations of the hypothalamus and pituitary gland....more »
    9. Ataxia, spastic with congenital miosis
     A rare disorder characterized by movement problems of the limbs as well as an impaired pupil reaction to light (miosis)....more »
    10. Atherosclerosis, premature -- deafness -- diabetes mellitus -- photomyoclonus -- nephropathy -- degenerative neurologic disease
     A rare syndrome characterized mainly by deafness, diabetes, epilepsy, kidney disease and premature hardening of the arteries....more »
    11. Atherosclerosis- deafness -- diabetes -- epilepsy -- nephropathy
     A rare syndrome characterized mainly by deafness, diabetes, epilepsy, kidney disease and premature hardening of the arteries....more »
    12. Autism
     Childhood mental condition with social and communication difficulties....more »
    13. Battaglia Neri syndrome
     A very rare syndrome characterized by mental retardation, small head, epilepsy, coarse facial features and skeletal anomalies. Only two reported cases of this syndrome....more »
    14. Benign familial infantile epilepsy
     A harmless form of epilepsy that occurs during infancy. Psychomotor development is not affected....more »
    15. Birth Injury
     An injury to the mother caused by childbirth...more »
    16. Borud Syndrome
     A very rare syndrome characterized by numerous features including hearing and vision problems, heart muscle disease, ataxia and peripheral neuropathy....more »
    17. Brain cancer
     Cancer of the brain....more »
    18. Brain infection
     Infection of the brain including encephalitis...more »
    19. CDG syndrome type I
     A rare genetic disorder where the body is unable to synthesize glycoproteins which results in multisystem problems....more »
    20. Carbohydrate deficiency glycoprotein syndrome type II
     Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2 is caused by a genetic defect which involves t...more »
    21. Cerebellar abscess
     An abscess that forms in the part of the brain called the cerebellum. The abscess may result from other infections such as ear infections, dental abscess and lung infections. The prognosis is determined by the size and exact location of the abscess...more »
    22. Cerebellar ataxia, X-linked
     A disorder where degeneration of certain parts of the brain results in symptoms such as ataxia. The rate of progression can vary....more »
    23. Cerebellar degeneration, subacute
     A rare disorder involving degeneration of the cerebellum and sometimes involves nearby spinal cord or brain tissue....more »
    24. Cerebral Palsy
     Any brain disorder causing movement disability...more »
    25. Chorea familial benign
     A rare movement disorder which is stable and involves abnormal involuntary movements (chorea) and continuous writhing movements....more »
    26. Chromosome 15q triplication syndrome
     A rare chromosomal disorder where there are three copies of a part of the long arm of chromosome 15 resulting in various anomalies....more »
    27. Chromosome 15q13.3 microdeletion syndrome
     A genetic disorder characterized by the deletion of a small portion of genetic material at the chromosomal location of 15q13.3. A rare syndrome characterized mainly by seizures, mental retardation, and slightly unusual facial features....more »
    28. Chromosome 20 ring
     A rare chromosomal disorder where genetic material from one or both ends of chromosome 20 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic mate...more »
    29. Chromosome 4, trisomy 4p
     A rare chromosomal disorder where a portion of chromosome four is duplicated so there is three copies of it instead of the normal two....more »
    30. Concussion
     Brain injury causing loss of consciousness and bruising of the brain...more »
    31. Congenital disorder of glycosylation type 1K
     Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type Ik is caused by a defect on chromosome 16p13.3 a...more »
    32. Congenital disorder of glycosylation type 2E
     Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2e is caused by a defect on chromosome 16p and i...more »
    33. Continuous spike-wave during slow sleep syndrome
     A rare form of epilepsy that occurs between the ages of 3 and 7 and is diagnosed by the observation through an EEG of continuous spike and wave discharges during the slow sleep phase which is detected. The seizures often occur during sleep. Children outgr...more »
    34. Cornelia de Lange syndrome 2
     A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. Type 2 is not as severe as type 1 with some of the abnormalities not presenting until later in life or absent altogether. The range a...more »
    35. Cortical dysplasia -- focal epilepsy syndrome
     Abnormal development of the brain cortex which results in focal epilepsy and progressive neurological deterioration once the epilepsy starts in early childhood....more »
    36. Craniodiaphyseal dysplasia
     A very rare bone disorder where excess calcium is deposited mainly in the skull bones which can result in compression of various nerves in the skull and even the brain....more »
    37. De Lange 1
     A rare disorder involving a variety of congenital abnormalities including retarded growth, behavioral problems, characteristic facial features and upper limb abnormalities....more »
    38. Deafness -- onychodystrophy -- osteodystrophy -- mental retardation
     A very rare inherited disorder involving deafness (D), onychodystrophy (O - nail malformation), osteodystrophy (O - bone malformation) and mental retardation (R)....more »
    39. Deafness, congenital onychodystrophy, recessive form
     A very rare inherited disorder involving deafness (D), onychodystrophy (O - nail malformation), osteodystrophy (O - bone malformation) and mental retardation (R)....more »
    40. Developmental delay -- epilepsy -- neonatal diabetes
     A rare syndrome characterized mainly by developmental delay, epilepsy and early-onset diabetes....more »
    41. Diomedi-Bernardi-Placidi syndrome
     A very rare syndrome characterized mainly by epilepsy, mental retardation and progressive leg weakness and spasticity....more »
    42. Double cortex syndrome
     A rare brain development disorder which causes mental retardation and epilepsy. An extra layer of nerves develops under the brain cortex....more »
    43. Dup (2) (q11.2-q13)
     A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree....more »
    44. Dup (3) (pter-p24.3) and del (7) (pter-p22.1)
     A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree....more »
    45. Electrolyte abnormality
     An imbalance in the level of any of a number of chemicals (electrolytes) in the blood stream e.g. chloride, sodium, magnesium, potassium, calcium, phosphate and bicarbonate. Symptoms can vary depending on which electrolyte is involved and the severity of ...more »
    46. Encephalitis
     Dangerous infection of the brain...more »
    47. Encephalopathy, familial, with neuroserpin inclusion bodies
     A rare neurodegenerative disorder involving brain disease due to a genetic chemical abnormality which results in the abnormal deposit of neuroserpin inclusion bodies which is harmful to the nerves....more »
    48. Epilepsy -- mental deterioration, Finnish type
     A rare disorder that occurs predominantly in people of Finnish origin and is characterized by the association of epilepsy with mental retardation....more »
    49. Epilepsy -- microcephaly -- skeletal dysplasia
     A rare syndrome characterized by epilepsy, a small head and skeletal abnormalities....more »
    50. Epilepsy occipital calcifications
     A rare disorder characterized by calcification of the occipital part of the brain, epilepsy. Celiac disease is also usually associated with the disorder....more »
    51. Epilepsy, idiopathic generalized
     A group of epileptic disorders that have genetic links and thus there is usually a family history of epilepsy. There are generally no other anomalies or structural brain abnormalities associated. Symptoms usually start between early childhood and adolesce...more »
    52. Epilepsy, idiopathic generalized, susceptibility to, 1
     A susceptibility to epilepsy linked to a particular gene - 8q24....more »
    53. Epilepsy, idiopathic generalized, susceptibility to, 2
     A susceptibility to epilepsy linked to a particular gene - 14q23....more »
    54. Epilepsy, idiopathic generalized, susceptibility to, 3
     A susceptibility to epilepsy linked to a particular gene - 9q32-q33....more »
    55. Epilepsy, idiopathic generalized, susceptibility to, 4
     A susceptibility to epilepsy linked to a particular gene - 10q25-q26....more »
    56. Epilepsy, idiopathic generalized, susceptibility to, 5
     A susceptibility to epilepsy linked to a particular gene - 10p11.22....more »
    57. Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
     A rare disorder characterized by epilepsy, writer's cramp seizures and sudden exercise-induced dystonia. The dystonia could occur in the neck, face, trunk or limbs. The writer's cramp tended to start during childhood and continue into adolescence....more »
    58. Epileptic encephalopathy, Lennox-Gastaut type
     A rare genetic disorder characterized by mental retardation and physical anomalies. The brain condition is progressive and results in loss of previously acquired skills....more »
    59. Erythrokeratodermia with ataxia
     A rare syndrome characterized by the association of a skin disorder with slowly progressive neurological symptoms....more »
    60. Familial porencephaly
     A very rare developmental abnormality that tends to run in families and is characterized by a localized accumulation of cerebrospinal fluid in the brain. The severity of symptoms is determined by the size and location of the brain abnormality....more »
    61. Febrile Seizures
     Fever-caused seizures in infants or children....more »
    62. Feigenbaum-Bergeron-Richardson syndrome
     A rare syndrome characterized mainly by deafness, diabetes, epilepsy, kidney disease and premature hardening of the arteries....more »
    63. Flynn-Aird syndrome
     A rare inherited disorder where neurological degeneration causes symptoms such as dementia, ataxia, eye problems, skin disorders and muscle wasting....more »
    64. Focal cortical dysplasia
     Abnormal development of the brain cortex which results in focal epilepsy and progressive neurological deterioration once the epilepsy starts in early childhood....more »
    65. Friedreich ataxia
     A progressive inherited neuromuscular disorder involving slow degeneration of the spinal cord and brain....more »
    66. Fryns-Aftimos syndrome
     A rare syndrome characterized mainly by abnormal brain development, epilepsy, mental retardation and unusual facial appearance....more »
    67. Fukuyama type muscular dystrophy
     A rare inherited muscle wasting disease occurring predominantly in Japan and characterized by mental retardation and muscle weakness from infancy....more »
    68. Gangliosidosis GM1 type 3
     A rare biochemical disorder involving a deficiency of an enzyme (beta-galactosidase A) which results in the accumulation of harmful chemicals (GM1 gangliosides) in the central nervous system and other body tissues. Type III involves a lesser degree of acc...more »
    69. Gangliosidosis, generalized GM1 type 3
     A rare biochemical disorder involving a deficiency of an enzyme (beta-galactosidase A) which results in the accumulation of harmful chemicals (GM1 gangliosides) in the central nervous system and other body tissues. Type III involves a lesser degree of acc...more »
    70. Gurrieri-Sammito-Bellussi syndrome
     A rare syndrome characterized by epilepsy, short stature and skeletal abnormalities....more »
    71. Heterotopia, Periventricular, Associated with Chromosome 5q Deletion
     A brain anomaly linked to a defect on chromosome 5q and characterized mainly by severe mental retardation and epilepsy....more »
    72. Hydroxyacyl-coa dehydrogenase, type 2, deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Some ...more »
    73. Hyperekplexia and epilepsy
     A rare genetic disorder characterized by progressively severe epilepsy and hyperekplexia. The condition is caused by a defect on chromosome Xq22.1....more »
    74. Hypoglycemia
     Low blood sugar level...more »
    75. Hypoparathyroidism X-linked
     Low parathyroid levels inherited in a X-linked manner and hence only males are symptomatic and females are asymptomatic carriers....more »
    76. Ichthyosis male hypogonadism
     A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads....more »
    77. Infant Cytomegalic virus
     A serious CMV viral infection in newborns....more »
    78. Injury
     Any damage inflicted in the body...more »
    79. Kohlschutter-Tonz syndrome
     A rare syndrome involving degeneration of the central nervous system, seizures and abnormal tooth development....more »
    80. Lipoid proteinosis of Urbach and Wiethe
     A rare congenital lipoid storage disease where lipids, carbohydrates and proteins are deposited onto blood vessel walls and other tissues....more »
    81. Lissencephaly, X-linked 2
     A rare brain malformation where the surface of the brain is smoother than normal. Genital anomalies are also associated. The severity of the disorder is variable....more »
    82. Liver disease -- retinitis pigmentosa -- polyneuropathy -- epilepsy
     An inherited disorder characterized by an enzyme (Alpha-methyl-acyl-CoA racemase) deficiency, liver disease, epilepsy, polyneuropathy and eye problems. The neuropathy tends to start during adulthood....more »
    83. MRXS-Christianson
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    84. McDowall syndrome
     A very rare syndrome characterized mainly by mental retardation and excessive skin folds and furrows on the scalp....more »
    85. Meningitis
     Dangerous infection of the membranes surrounding the brain....more »
    86. Mental retardation -- dysmorphism -- hypogonadism -- diabetes
     A very rare syndrome characterized mainly by mental retardation, hypogonadism, diabetes and facial and skull abnormalities....more »
    87. Mental retardation -- epilepsy
     A very rare syndrome characterized by the association of mental retardation with epilepsy....more »
    88. Mental retardation -- epilepsy -- bulbous nose
     A very rare syndrome characterized mainly by mental retardation, epilepsy and a bulbous nose. The condition has been reported in only two families....more »
    89. Mental retardation syndrome, Belgian type
     A rare form of mental retardation reported in a Belgian family....more »
    90. Mental retardation, Microcephaly, Epilepsy and Ataxia Syndrome
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    91. Mental retardation, X-linked -- craniofacial dysmorphology -- epilepsy -- ophthalmoplegia -- cerebellar atrophy
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    92. Mental retardation, X-linked, Wittwer type
     A rare disorder characterized by severe mental retardation, retarded growth, seizures and vision and hearing problems. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers ma...more »
    93. Mental retardation, X-linked, syndromic, due to JARID1C mutation
     A rare disorder characterized by mental retardation, spasticity and other variable features. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms...more »
    94. Microcephaly -- mental retardation -- spasticity -- epilepsy
     A very rare disorder characterized by an abnormally small head, mental retardation, spasticity and epilepsy....more »
    95. Microcephaly -- pontocerebellar hypoplasia -- dyskinesia
     A rare, recessively inherited disorder characterized by an abnormally small brain and brainstem which manifests as a small head and mental retardation. The brain progressively degenerates....more »
    96. Microencephaly
     Small brain. The condition is often characterized by a small head and neurological problems. The type and severity of symptoms are variable....more »
    97. Mowat-Wilson syndrome
     A very rare syndrome characterized mainly by mental retardation, a small head, characteristic facial appearance and various other abnormalities....more »
    98. Myoclonic progressive familial epilepsy
     A progressive familial disorder involving the central nervous system and manifesting as epilepsy and myoclonus (muscle contractions) that worsen over time....more »
    99. Myoclonus progressive epilepsy of Unverricht and Lundborg
     A rare genetic brain disease characterized by convulsions which become progressively worse. Modern treatment can have a big effect on the prognosis....more »
    100. Neurodegenerative syndrome, X-linked, Hamel type
     A very rare neurodegenerative disorder characterized mainly by mental retardation, blindness, convulsions, spasticity and early death. The disorder is X-linked and thus only males suffer the full extent of the symptoms whereas female carriers may be asymp...more »
    101. Neurofibromatosis Type 1 (NF-1)
     Neurofibromatosis Type 1 is a genetic disorder often leading to the development of nerve tumors. The condition is also characterized by skin pigmentation abnormalities....more »
    102. Neurofibromatosis-1
     Genetic disorder often leading to tumors on nerves....more »
    103. Nevus comedonicus syndrome
     A rare condition characterized by the development of large comedones which can occur in groups or linear arrangements. The skin lesions tend to occur mainly on the face, neck, arms and trunk. If it is associated with other congenital malformations, it is ...more »
    104. Nicolaides-Baraitser syndrome
     A very rare syndrome characterized mainly by short stature, reduced hair, short fingers, epilepsy and abnormal bone development....more »
    105. Niemann-Pick disease, type D
     Niemann-Pick disease is an inherited metabolic disorder where lipids are not able to be metabolized adequately and hence build up and cause damage in various parts of the body such as the spleen, liver, lungs, bone marrow and brain. Type D is no longer a ...more »
    106. OFD syndrome type IX
     A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger and retinal abnormalities....more »
    107. Olivopontocerebellar Atrophy
     A group of diseases progressive degeneration occurs in a particular area of the brain (olivopontocerebellar area) which results in various neurological symptoms....more »
    108. Onychodystrophy -- deafness
     A very rare inherited disorder involving deafness (D), onychodystrophy (O - nail malformation), osteodystrophy (O - bone malformation) and mental retardation (R)....more »
    109. Osler's disease
     Genetic disease causing multiple teleangiectasias...more »
    110. Peripheral type neurofibromatosis
    111. Perisylvian syndrome
     A very rare nerve disorder characterized by weakness or paralysis of face, jaw tongue and throat muscles. Other symptoms include seizures, delayed development and mental retardation....more »
    112. Phenylketonuria type 2
     A genetic condition where phenylalanine (component of protein) is unable to be broken down due to an enzyme (phenylalanine hydroxylase) deficiency which leads to a harmful build up of the compound. The condition is characterized by neurological symptoms a...more »
    113. Photosensitive epilepsy
     Epilepsy or seizures triggered by visual stimuli such as flashing light, moving patterns and bold, regular patterns....more »
    114. Pitt-Hopkins syndrome
     A very rare syndrome characterized mainly by mental retardation with periods of overbreathing and apnea....more »
    115. Poisoning
     The condition produced by poison...more »
    116. Polymicrogyria, Bilateral Frontal
     Polymicrogyria refers to abnormal brain development where the brain has abnormally smooth gyri (convolutions) on the surface of the brain. The anomaly is often occurs as part of another syndrome. Patients can present with a wide range and severity of symp...more »
    117. Pontocerebellar Hypoplasia Type 2B
     A rare inherited condition where the brainstem and part of the brain (cerebellum) is abnormally small. Type 2B differs from other types with respect to the location of the genetic defect....more »
    118. Pontocerebellar Hypoplasia Type 2C
     A rare inherited condition where the brainstem and part of the brain (cerebellum) is abnormally small. Type 2C differs from other types with respect to the location of the genetic defect....more »
    119. Pontocerebellar hypoplasia with infantile spinal muscular atrophy
     A rare, recessively inherited disorder characterized by an abnormally small brain and brainstem which manifests as a small head and mental retardation. The disorder is lethal with death usually occurring within the first year. The brain progressively dege...more »
    120. Porencephaly
     A central nervous system disorder involving cysts in the brain cortex caused by stroke, infection or genetic anomaly....more »
    121. Renier-Gabreels-Jasper syndrome
     A very rare inherited syndrome characterized by a small head, severe mental retardation, spasticity, deafness and epilepsy....more »
    122. Rett's syndrome
     Autism-like behavioral syndrome in infant girls...more »
    123. Rud Syndrome
     A condition characterized by ichthyosis, epilepsy, short stature, hypogonadism and severe mental retardation....more »
    124. SCHAD deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    125. Schaefer-Stein-Oshman syndrome
     A rare disorder where excessive growth and abnormal hardening affects the head and facial bones....more »
    126. Segawa syndrome, autosomal recessive
     A very rare birth disorder characterized mainly by involuntary jerky movements that start during infancy. The disorder is caused by a genetic defect resulting in a deficiency of an enzyme called tyrosine hydroxylase. The disorder is usually treatable by a...more »
    127. Single upper central incisor
     A very rare syndrome characterized by various defects in the middle of the face....more »
    128. Spastic paraplegia epilepsy mental retardation
     A very rare syndrome characterized mainly by epilepsy, mental retardation and progressive leg weakness and spasticity....more »
    129. Spastic tetraplegic -- cerebral palsy
     A rare disorder characterized by the association of spasticity (muscle tightness of the arms and legs as well as cerebral palsy....more »
    130. Spasticity -- mental retardation -- epilepsy, X-linked
     A rare syndrome characterized by epilepsy, spasticity and mental retardation. The disorder is inherited in a X-linked manner and thus only males present with symptoms though female carriers may have some mild symptoms such as hyperreflexia....more »
    131. Spinocerebellar Ataxia
     A condition characterised by a failure of muscle coordination due to pathology arising in the spinocerebellar tract of the spinal cord...more »
    132. Spinocerebellar ataxia 10
     A rare genetic disorder (chromosome 22q13 defect) characterized by gait ataxia and dysarthria (speech disorder). The severity of the condition is variable with some patients becoming wheelchair dependent....more »
    133. Spinocerebellar ataxia 11
     A rare genetic disorder (chromosome 15q14-21.3 defect) characterized by gait ataxia and dysarthria (speech disorder). This form of the condition progresses slowly and doesn't affect life expectancy....more »
    134. Spinocerebellar ataxia 12
     A rare genetic disorder (chromosome 5q31-q33 defect) characterized by variable symptoms such as arm tremors, gait ataxia and dysarthria (speech disorder) with other....more »
    135. Spinocerebellar ataxia 13
     A rare genetic disorder (chromosome 19 defect) characterized by progressive mental retardation. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    136. Spinocerebellar ataxia 14
     A rare genetic disorder (chromosome 19q13.4qter defect) characterized by gait ataxia, tremors and dysarthria (speech disorder). The condition progresses slowly....more »
    137. Spinocerebellar ataxia 15
     A rare genetic disorder (chromosome 3p26-p25 defect) characterized by gait ataxia, eye movement problems and dysarthria (speech disorder). The condition tends to progress slowly over decades with most patients retaining the ability to walk....more »
    138. Spinocerebellar ataxia 16
     A rare genetic disorder (chromosome 3p26.2-pter defect) characterized by gait ataxia, eye movement problems, tremor and dysarthria (speech disorder). The progression of the condition is variable (1-40 years)....more »
    139. Spinocerebellar ataxia 17
     A rare genetic disorder (chromosome 6q27 defect) characterized by . Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    140. Spinocerebellar ataxia 18
     A rare genetic disorder (chromosome 7q22-31 defect) characterized by muscle atrophy and sensory loss. The severity of symptoms is variable. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia t...more »
    141. Spinocerebellar ataxia 19
     A rare genetic disorder (chromosome 1p21-q21 defect) characterized by mild cognitive impairment and myoclonus. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    142. Spinocerebellar ataxia 20
     A rare genetic disorder (chromosome 11 defect) characterized by palatal tremor and dysphonia. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    143. Spinocerebellar ataxia 21
     A rare genetic disorder (chromosome 7p21.3-p15.1 defect) characterized by extrapyramidal features and cognitive impairment. The condition progresses slowly over decades. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to al...more »
    144. Spinocerebellar ataxia 23
     A rare genetic disorder (chromosome 20p13-12.3 defect) characterized by ataxia, sensory loss and pyramidal signs. It is a slowly progressing condition....more »
    145. Spinocerebellar ataxia 25
     A rare genetic disorder (chromosome 2p15-p21 defect) characterized by sensory neuropathy and damage to the motor control part of the brain (cerebellar atrophy) resulting in ataxia. It is a slow progressing condition....more »
    146. Spinocerebellar ataxia 26
     A rare genetic disorder (chromosome 19p13.3 defect) characterized by slowly progressive ataxia and dysarthria (speech disorder)....more »
    147. Spinocerebellar ataxia 27
     A rare genetic disorder (chromosome FGF14; 13q34 defect) characterized by tremors, dyskinesia and psychiatric episodes. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    148. Spinocerebellar ataxia 28
     A rare genetic disorder (chromosome 18p11 defect) characterized by eye muscle paralysis (ophthalmoplegia) and increased reflexes. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    149. Spinocerebellar ataxia 3
     A rare genetic disorder (chromosome 14q32.1defect) characterized by . Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types. The duration of the disease is 1-20 years....more »
    150. Spinocerebellar ataxia 5
     A genetic disorder involving progressive degeneration of the spinal cord resulting in symptoms such as incoordination and eye movement problems....more »
    151. Spinocerebellar ataxia 8
     A rare genetic disorder (chromosome 13q21 defect) characterized by horizontal nystagmus and mild sensory neuropathy. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    152. Spinocerebellar ataxia, Machado-Joseph type I
     A rare genetic disorder (chromosome 14q32.1defect) characterized by early onset of symptoms - ataxia, bulging eyes and extrapyramidal symptoms. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar atax...more »
    153. Spinocerebellar ataxia, Machado-Joseph type II
     A rare genetic disorder (chromosome 14q32.1defect) characterized by intermediate onset of symptoms. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    154. Spinocerebellar ataxia, Machado-Joseph type III
     A rare genetic disorder (chromosome 14q32.1defect) characterized by later onset of symptoms such as weak eye muscles and peripheral neuropathy. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar atax...more »
    155. Spinocerebellar ataxia, Machado-Joseph type IV
     A rare genetic disorder (chromosome 14q32.1defect) characterized by late onset of symptoms - muscle twitching and Parkinsonism. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    156. Spinocerebellar ataxia, Machado-Joseph type V
     A rare genetic disorder (chromosome 14q32.1defect) characterized by spastic paraparesis. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types....more »
    157. Spinocerebellar ataxia, autosomal recessive 1
     A neurological disorder characterized by progressive ataxia, tremor and muscle weakness and wasting. The rate of progression and severity is variable with some needing wheelchairs in their second decade and others still capable of some walking in their 4t...more »
    158. Spinocerebellar ataxia, autosomal recessive 6
     A rare disorder that has neurological origins and causes nonprogressive ataxia, which begins during infancy....more »
    159. Spinocerebellar ataxia, autosomal recessive 7
     A rare, recessively inherited neurological disorder caused by abnormalities in the cerebellum and spinal cord. The severity of the disorder is variable....more »
    160. Spinocerebellar ataxia, autosomal recessive 9
     A rare, recessively inherited neurological disorder caused by abnormalities in the cerebellum and spinal cord. This particular form of the condition is caused by a defect in the CABC1 gene on chromosome 1q42.2....more »
    161. Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
     A rare neurological disorder caused by a genetic defect (chromosome 114q31-q32, recessive) and resulting in ataxia and dysarthria....more »
    162. Stroke
     Serious brain event from bleeding or blood clots....more »
    163. Subependymal nodular heterotopia
     A rare inherited disorder where a part of the brain tissue is misplaced during development. More specifically, nodules of the abnormal tissue is found in the subependymal part of the brain....more »
    164. Traumatic Brain Injury
     Brain injury from trauma or accident....more »
    165. Type 10 17b-hydroxysteroid dehydrogenase deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    166. WAGR Syndrome
     A syndrome that is due to the deletion of chromosome 11....more »
    167. Wilms tumor -- aniridia -- genitourinary anomalies -- mental retardation
     A syndrome resulting from deletion of genetic material from chromosome the short arm of chromosome 11 (11p13). The characteristic symptoms are partial or complete absence of iris, genitourinary anomalies, mental retardation and Wilms' tumor. The specific ...more »
    168. Wittwer sydnrome
     A syndrome that is characterised by the occurrence of growth retardation, blindness, hearing loss, dysmorphic features, epilepsy, mental retardation and the absence of speech...more »

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