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Results 1 - 10 of 11 for Small basal ganglia
  1. Autosomal dominant hypocalcemia 
    ... form in the brain, typically in structures called basal ganglia, which help control movement.A small percentage of severely affected individuals have features of ...
    https://medlineplus.gov/.../autosomal-dominant-hypocalcemia - Genetics
  2. TUBB4A-related leukodystrophy 
    ... of hypomyelination and atrophy or impairment of the basal ganglia or other brain regions. Movement problems can also occur. A small group of affected individuals develop muscle stiffness and ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  3. SLC19A3 gene 
    ... and symptoms overlap those of biotin-thiamine-responsive basal ganglia ... (atrophy). A small number of individuals with signs and symptoms similar ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  4. Myoclonus-dystonia 
    ... in coordinating and controlling movements (the cerebellum and basal ... genes cause a small percentage of cases. These genes are primarily active ( ...
    https://medlineplus.gov/genetics/condition/myoclonus-dystonia - Genetics
  5. Glutaric acidemia type I 
    ... and cause damage to the brain, particularly the basal ganglia, which are ... but in a small number of affected individuals, the disorder first becomes ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  6. Primary familial brain calcification 
    ... on medical imaging and typically occur in the basal ganglia, which are structures deep within the brain that ... brain calcification by disrupting the connections between the basal ganglia and other areas of the brain, particularly the ...
    https://medlineplus.gov/.../primary-familial-brain-calcification - Genetics
  7. Aicardi-Goutières syndrome 
    ... AGS Aicardi Goutieres syndrome Cree encephalitis Encephalopathy with basal ganglia calcification Familial infantile encephalopathy with intracranial calcification and ...
    https://medlineplus.gov/.../condition/aicardi-goutieres-syndrome - Genetics
  8. TAF1 gene 
    The TAF1 gene provides instructions for making part of a protein called transcription factor IID (TFIID). This protein is active in cells and tissues throughout ...
    https://medlineplus.gov/genetics/gene/taf1 - Genetics
  9. RGS9 gene 
    The RGS9 gene provides instructions for making two versions (isoforms) of the RGS9 protein, known as RGS9-1 and RGS9-2. They are found in different parts ...
    https://medlineplus.gov/genetics/gene/rgs9 - Genetics
  10. Leigh syndrome 
    ... regions of the brain. These regions include the basal ganglia, which help control movement; the cerebellum, which controls ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
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