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Intellectual "disability," autosomal dominant 34
- ... may have mild to severe developmental delay and intellectual disability. Affected individuals may also have seizures, an unusually ... the KMT2D gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... Dravet syndrome have difficulty coordinating movements (ataxia) and intellectual disability.Some people with GEFS+ have seizure disorders of ... GABRG2 SCN1B STX1B GEFS+ is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... syndrome range from normal to mild or moderate intellectual disability.Individuals with Apert syndrome have syndactyly of the ... feet. FGFR2 Apert syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... These structural changes can cause mild to severe intellectual disability, developmental delay, and seizures.Other features of Baraitser- ... syndrome. ACTB ACTG1 This condition is described as autosomal dominant, which means one copy of the altered gene ...
- ... condition. In other cases, the condition has an autosomal dominant pattern of inheritance, which means one copy of ...
