Results 11 -
20
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49
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Intellectual "disability," autosomal dominant 30
- ... methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability. Nat Genet. 2014 Apr;46(4):385-8. ...
- ... large head size (macrocephaly), a variable degree of intellectual disability (usually mild), and characteristic facial features. These features ... the relationship between these brain abnormalities and the intellectual disability associated with Weaver syndrome is unclear.Researchers suggest ...
- ... condition characterized by abnormal brain function (encephalopathy) and intellectual disability. Most affected individuals also have recurrent seizures (epilepsy). ...
- ... growth and speech development, and some have mild intellectual disability or learning disabilities. Older affected individuals have difficulty ... the 22q11.2 deletion were diagnosed with the autosomal dominant form of Opitz G/BBB syndrome and Cayler ...
- ... before and after birth leading to short stature; intellectual disability that is usually moderate to severe; and abnormalities ... those with HDAC8 gene variants may have significant intellectual disability.In about 15 percent of cases, the cause ...
- ... small percentage of affected individuals have delayed development, intellectual disability, or autism spectrum disorder, which can affect communication ...
- ... Some affected individuals also have learning difficulties or intellectual disability.Thyroid problems are the next most common feature ... Although a shortage of thyroid hormones can cause intellectual disability and other neurological problems, it is unclear whether ...
- ... 22q13.3 deletion syndrome, such as developmental delay, intellectual disability, and absent or severely delayed speech. Additional genes ... disrupts the normal course of development, leading to intellectual disability and birth defects. Researchers are working to determine ...
- ... disorder that is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial ...
- ... Rarely, people with combined pituitary hormone deficiency have intellectual disability; a short, stiff neck; or underdeveloped optic nerves, ... the disorder is familial, it can have an autosomal dominant or an autosomal recessive pattern of inheritance.Autosomal ...
