Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 46 for Corpus "callosum," agenesis of
  1. ... development. DBS DBS/FOAR syndrome Diaphragmatic hernia-exomphalos-corpus callosum agenesis Diaphragmatic hernia-exomphalos-hypertelorism syndrome Faciooculoacousticorenal syndrome FOAR ...
  2. ... anomalies with ACC Genetic Testing Registry: Aicardi syndrome Corpus callosum agenesis National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
  3. ... Agenesis of the corpus callosum with peripheral neuropathy Corpus callosum agenesis-neuronopathy syndrome National Organization for Rare Disorders (NORD) ...
  4. ... 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) ...
  5. ... MRX43 MRX54 MRXS1 PRTS Tests of ARX PubMed CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA INTELLECTUAL DEVELOPMENTAL DISORDER, X- ...
  6. ... of the condition. Absent corpus callosum cataract immunodeficiency Corpus callosum agenesis-cataract-immunodeficiency syndrome Dionisi Vici Sabetta Gambarara syndrome ...
  7. ... 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 ...
  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, ...
previous · 1 · 2 · 3 · 4 · 5 · next