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Bookmark or Share- Aicardi syndrome | About the Disease | GARD - Genetic and Rare Diseases ...A rare neurodevelopmental disorder characterized by the classic triad of agenesis of the corpus callosum (total or partial), central chorioretinal lacunae and infantile spasms that affects almost exclusively females. Summary.
- Aicardi syndrome - WikipediaAicardi 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 lacunes, and epileptic seizures in the form of infantile spasms. [2]
- Aicardi Syndrome: What It Is, Causes, Symptoms & TherapiesWhat is Aicardi syndrome? Aicardi syndrome is a rare disorder that’s present at birth (congenital). It causes malformations in the brain, eyes and other parts of the body. It leads to lifelong difficulties, including intellectual disabilities and developmental delay.
- Aicardi syndrome - MedlinePlusAicardi syndrome is a disorder that occurs almost exclusively in females. It is characterized by three main features that occur together in most affected individuals. People with Aicardi syndrome have absent or underdeveloped tissue connecting the left and right halves of the brain (agenesis or dysgenesis of the corpus callosum ).
- Aicardi Syndrome: Causes, Symptoms and Diagnosis - HealthlineAicardi syndrome is a rare genetic disorder that interferes with the formation of the corpus callosum, which is the structure that connects the two sides of the brain.
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