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Symptom Checker » Abnormal Babinski's reflex » Basal ganglia symptoms
 

Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness
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Contents
  1. Abnormal Babinski's reflex AND Basal ganglia symptoms AND Emotional lability AND Movement symptoms AND Speaking difficulty with numbness: Causes of All Symptoms
  2. Abnormal Babinski's reflex OR Basal ganglia symptoms OR Emotional lability OR Movement symptoms OR Speaking difficulty with numbness: 5832 causes
  3. Abnormal Babinski's reflex: Causes
  4. Abnormal Babinski's reflex: Introduction
  5. Basal ganglia symptoms: Causes
  6. Basal ganglia symptoms: Introduction
  7. Emotional lability: Causes
  8. Emotional lability: Introduction
  9. Movement symptoms: 5821 causes
  10. Movement symptoms: Introduction
  11. Speaking difficulty with numbness: Causes
  12. Speaking difficulty with numbness: Introduction
  13. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Abdominal symptoms (2 causes)
  14. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Abnormal eye movements (2 causes)
  15. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Abnormal patellar reflex (2 causes)
  16. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Abnormal rigidity (2 causes)
  17. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Acute brain injury (2 causes)
  18. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Aphasia (2 causes)
  19. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Arm paresthesia (2 causes)
  20. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Arm symptoms (2 causes)
  21. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Ataxia (2 causes)
  22. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and Ataxia due to CNS disorders (2 causes)
  23. Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness and MORE SYMPTOMS

Abnormal Babinski's reflex and Basal ganglia symptoms and Emotional lability and Movement symptoms and Speaking difficulty with numbness

  • Abnormal Babinski's reflex AND Basal ganglia symptoms AND Emotional lability AND Movement symptoms AND Speaking difficulty with numbness - Causes of All Symptoms
  • Abnormal Babinski's reflex OR Basal ganglia symptoms OR Emotional lability OR Movement symptoms OR Speaking difficulty with numbness - 5832 causes

Abnormal Babinski's reflex:

Basal ganglia symptoms:

Emotional lability:

Movement symptoms:

Speaking difficulty with numbness:

Results: Causes of Abnormal Babinski's reflex AND Basal ganglia symptoms AND Emotional lability AND Movement symptoms AND Speaking difficulty with numbness

Results: 5832 causes of Abnormal Babinski's reflex OR Basal ganglia symptoms OR Emotional lability OR Movement symptoms OR Speaking difficulty with numbness

    1. 10q Partial Trisomy
     A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary consider...more »
    2. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    3. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    4. 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 »
    5. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    6. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    7. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    8. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    9. 3 alpha methylglutaconicaciduria, type 3
     A rare genetic condition where a gene mutation prevents the production of certain protein which leads to a build-up of an acid (3-methylglutaconic acid) which can have a negative impact on the body. The condition is characterized mainly by damage to the o...more »
    10. 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency
     A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable....more »

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Notes About Causes

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