corpus callosum syndrome

  • 1Corpus callosum — For the two films with this name, see Corpus Callosum (2002) and Corpus Callosum (2007) Brain: Corpus callosum Corpus callosum from above. (Anterior portion is at the top of the image.) …

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  • 2Corpus callosum, agenesis of the — A congenital abnormality (a birth defect) in which there is partial or complete absence (agenesis) of the corpus callosum, the area of the brain which connects the two cerebral hemispheres (the two halves of the brain). Agenesis of the corpus… …

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  • 3Agenesis of the corpus callosum — Classification and external resources OMIM 217990 DiseasesDB 29900 eMedicine …

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  • 4Syndrome d'Andermann — Référence MIM 218000 Transmission Récessive Chromosome 15q13 q14 Gène SLC12A6 Mutation Ponctuelle …

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  • 5Alien hand syndrome — Classification and external resources ICD 9 781.8 MeSH D055964 Alien hand syndrome ( …

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  • 6Lujan-Fryns syndrome — Lujan–Fryns syndrome Classification and external resources Lujan–Fryns syndrome in a young adult male, with features that include a long, narrow face and recessed chin. ICD 10 F …

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  • 7Fetal alcohol syndrome — (FAS) is a disorder of permanent birth defects that occurs in the offspring of women who drink alcohol during pregnancy. It is unknown whether amount, frequency or timing of alcohol consumption during pregnancy causes a difference in degree of… …

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  • 8Aicardi syndrome — is a rare genetic malformation syndrome characterized by the partial or complete absence of a key structure in the brain called the corpus callosum, the presence of retinal abnormalities, and seizures in the form of infantile spasms. Aicardi… …

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  • 9Vici syndrome — is a rare autosomal recessive congenital disorder characterized by albinism, agenesis of the corpus callosum, cataracts, cardiomyopathy, severe psychomotor retardation, seizures, immunodeficiency, and recurrent severe infections.cite journal… …

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  • 10MASA syndrome — Classification and external resources OMIM 303350 MASA syndrome, also called CRASH syndrome and Gareis Mason syndrome,[1] is a rare X linked recessive[2 …

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