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Symptom Checker » Acute disorientation » Concentration difficulty
 

Acute disorientation and Concentration difficulty and Excessive hunger in children and Nystagmus and Sudden onset of convulsions in newborn
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Acute disorientation and Concentration difficulty and Excessive hunger in children and Nystagmus and Sudden onset of convulsions in newborn

  • Acute disorientation AND Concentration difficulty AND Excessive hunger in children AND Nystagmus AND Sudden onset of convulsions in newborn - Causes of All Symptoms
  • Acute disorientation OR Concentration difficulty OR Excessive hunger in children OR Nystagmus OR Sudden onset of convulsions in newborn - 732 causes

Acute disorientation:

Concentration difficulty:

Excessive hunger in children:

Nystagmus:

Sudden onset of convulsions in newborn:

Results: Causes of Acute disorientation AND Concentration difficulty AND Excessive hunger in children AND Nystagmus AND Sudden onset of convulsions in newborn

Note: Do not use for diagnosis; see limitations of results.

Results: 732 causes of Acute disorientation OR Concentration difficulty OR Excessive hunger in children OR Nystagmus OR Sudden onset of convulsions in newborn

    1. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...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. 8p-Syndrome, partial
     A rare chromosomal disorder where there is one copy of part of the short arm (p) of chromosome 8 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material deleted....more »
    4. Abetalipoproteinemia
     A rare disorder involving abnormalities in fat metabolism. The resulting insufficiency of fats and vitamins affect the normal development and function of the body....more »
    5. Ablinism I syndrome
     A recessively inherited form of albinism involving the complete lack of skin, hair and eye pigments....more »
    6. Absence of septum pellucidum and septo-optic dysplasia
     A rare birth defect where a thin membrane in the middle of the brain is missing. This brain abnormality is never present on it's own but is a characteristic of septo-optic dysplasia where the patient also has optic disk abnormalities and pituitary deficie...more »
    7. Absence of septum pellucidum with porencephalia syndrome
     A rare syndrome present at birth and characterized by the absence of the thin membrane in the middle of the brain (septum pellucidum) as well as abnormal cavities in the brain (porencephaly). The syndrome also involves other structural brain abnormalities...more »
    8. Acanthocytosis
     A rare disorder where most of the red blood cells are abnormal with spiny projections due to lipid abnormalities. The blood abnormality is seen in conditions such as abetalipoproteinemia, severe liver disease and severe malnutrition. Symptoms and prognosi...more »
    9. Achard syndrome
     An inherited connective tissue disorder characterized primarily by a short head, long, slender bones, recessed lower jaw and loose hand and foot joints....more »
    10. Achrestic anemia
     Achrestic anemia is a form of anemia similar to that caused by Vitamin B12 deficiency but it doesn't respond to treatment with Vitamin B12. The condition tends to progress slowly and can result in death if not treated. There are a variety of possible caus...more »

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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
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