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Results 1 - 10 of 45 for Corpus "callosum," agenesis of
  1. ... of the condition. Absent corpus callosum cataract immunodeficiency Corpus callosum agenesis-cataract-immunodeficiency syndrome Dionisi Vici Sabetta Gambarara syndrome ...
  2. ... development. DBS DBS/FOAR syndrome Diaphragmatic hernia-exomphalos-corpus callosum agenesis Diaphragmatic hernia-exomphalos-hypertelorism syndrome Faciooculoacousticorenal syndrome FOAR ...
  3. ... spastic paraplegia type 1, and X-linked complicated corpus callosum agenesis.HSAS is an acronym for the characteristic features ... in structures of the brain.X-linked complicated corpus callosum agenesis is defined by underdevelopment (hypoplasia) or absence (agenesis) ...
  4. ... Agenesis of the corpus callosum with peripheral neuropathy Corpus callosum agenesis-neuronopathy syndrome National Organization for Rare Disorders (NORD) ...
  5. ... MRX43 MRX54 MRXS1 PRTS Tests of ARX PubMed CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA INTELLECTUAL DEVELOPMENTAL DISORDER, X- ...
  6. ... rare condition characterized by a brain abnormality called agenesis of the corpus callosum, the presence of extra fingers and toes (polydactyly), ... and their severity varies widely among affected individuals.Agenesis of the corpus callosum occurs when the tissue that connects the left ...
  7. ... have a condition called Klinefelter syndrome. Agenesis of corpus callosum with chorioretinal abnormality Agenesis of corpus callosum with infantile spasms and ...
  8. ... large head, imperforate anus, congenital hypotonia, and partial agenesis of the corpus callosum OKS Opitz-Kaveggia syndrome Genetic Testing Registry: FG ...
  9. ... Andrieux J, Dieux A, Tommerup N, Bache I. Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients ...
  10. Mowat-Wilson syndrome is a genetic condition that affects many parts of the body. Major signs of this disorder frequently include distinctive facial features, ...
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