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Results 1 - 10 of 42 for Hypoplasia of the corpus callosum
  1. Aicardi syndrome 
    Aicardi syndrome is a rare disorder. In this condition, the structure that connects the two sides of the brain (called the corpus callosum) ...
    https://medlineplus.gov/ency/article/001664.htm - Medical Encyclopedia
  2. L1 syndrome 
    ... to their sons. Adducted thumbs-mental retardation syndrome Corpus callosum hypoplasia, mental retardation, adducted thumbs, spastic paraplegia, hydrocephalus syndrome ...
    https://medlineplus.gov/genetics/condition/l1-syndrome - Genetics
  3. Acrocallosal syndrome 
    ... is a rare condition characterized by a brain abnormality called agenesis of the corpus callosum, the presence of extra fingers and toes (polydactyly), ...
    https://medlineplus.gov/genetics/condition/acrocallosal-syndrome - Genetics
  4. Pol III-related leukodystrophy 
    ... oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because these disorders were later found to ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  5. Aicardi syndrome 
    ... Klinefelter syndrome. Agenesis of corpus callosum with chorioretinal abnormality Agenesis of corpus callosum with infantile spasms and ocular abnormalities Aicardi's ...
    https://medlineplus.gov/genetics/condition/aicardi-syndrome - Genetics
  6. Combined oxidative phosphorylation deficiency 1 
    ... that connects the two halves of the brain (corpus callosum hypoplasia) and loss of brain tissue called white matter ( ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  7. ARID1B gene 
    ... Andrieux J, Dieux A, Tommerup N, Bache I. Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients ...
    https://medlineplus.gov/genetics/gene/arid1b - Genetics
  8. AKT3 gene 
    ... defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of ...
    https://medlineplus.gov/genetics/gene/akt3 - Genetics
  9. POLR3B gene 
    ... oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because these disorders were later found to ...
    https://medlineplus.gov/genetics/gene/polr3b - Genetics
  10. POLR3A gene 
    ... oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because these disorders were later found to ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
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