Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Corpus callosum, agenesis of

MONDO:0009022

A congenital abnormality characterized by the complete absence of the corpus callosum. It may be an isolated abnormality or associated with other central nervous system abnormalities or syndromes. Clinical manifestations vary. In cases of isolated corpus callosum agenesis, symptoms may be absent or minimal. In cases that are associated with other central nervous system abnormalities or syndromes, symptoms include developmental delays, motor coordination difficulties, and vision impairment.

Also known as: agenesis of corpus callosum, corpus callosum agenesis, corpus callosum, agenesis of, ACC, agenesis of the corpus callosum, isolated corpus callosum agenesis

4 clinical trials for this condition and its sub-types, 4 tagged with Corpus callosum, agenesis of itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of Corpus callosum, agenesis of

Sort by