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Intellectual "disability," autosomal dominant 13
- ... 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 ...
- ... growth of the brain, causing delayed development and intellectual disability.A skin abnormality called cutis gyrata is also ... unknown. FGFR2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... the brain cause seizures, profound developmental delay, and intellectual disability. Several affected individuals also have had episodes in ... causes acanthosis nigricans. FGFR3 SADDAN is considered an autosomal dominant disorder because one mutated copy of the FGFR3 ...
- ... people with nonsyndromic holoprosencephaly have developmental delay and intellectual disability. Affected individuals also frequently have a malfunctioning pituitary ...
- ... features of Kleefstra syndrome include developmental delay and intellectual disability, severely limited or absent speech, and weak muscle ... inheritance of Kleefstra syndrome is considered to be autosomal dominant because a deletion in one copy of chromosome ...
- ... or ADAR gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... syndrome. SMAD4 Myhre syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... symptoms. HRAS This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... the KMT2D gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... 2 deletion syndrome usually have developmental delay and intellectual disability. Most also have at least some features of ... 2 deletion syndrome is considered to have an autosomal dominant inheritance pattern because a deletion in one copy ...
