Results 91 -
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135
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Intellectual "disability," autosomal dominant 10
- ... individuals have some level of developmental delay and intellectual disability. Their cognitive functioning typically declines over time. Alternating ...
- ... constipation. If untreated, congenital hypothyroidism can lead to intellectual disability and slow growth. In the United States and ... TSHR or DUOX2 gene, the condition has an autosomal dominant pattern of inheritance, which means one copy of ...
- ... serious medical problems including seizures, delayed development, and intellectual disability. This condition is very rare; its prevalence is ... chromosome 7 This condition is inherited in an autosomal dominant pattern, which means one altered or missing copy ...
- ... with Bohring-Opitz syndrome have profound to severe intellectual disability, developmental delay, and seizures. Most affected individuals have ... condition. ASXL1 Bohring-Opitz syndrome is considered an autosomal dominant condition, 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 ...
- ... microcephaly). This underdevelopment of the brain causes severe intellectual disability, delayed development, and recurrent seizures (epilepsy) in individuals ...
- ... such as sitting, crawling, walking, and speaking, and intellectual disability that can range from mild to severe. In ... 18q deletion syndrome is considered to be an autosomal dominant condition. This means that a deletion in one ...
- ... people with nonsyndromic holoprosencephaly have developmental delay and intellectual disability. Affected individuals also frequently have a malfunctioning pituitary ...
- ... 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 ...
