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Intellectual "disability," autosomal dominant 50
- ... autism spectrum disorder ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder Helsmoortel-van der Aa syndrome HVDAS Mental retardation, autosomal dominant 28 MRD28 Genetic Testing Registry: ADNP-related multiple ...
- ... had abnormal calcium deposits (calcifications) in the brain, intellectual disability, and a form of kidney disease called renal tubular acidosis. Autosomal dominant osteopetrosis is the most common form of the ...
- ... extra copy of the RAI1 gene leads to intellectual disability and the other signs and symptoms of this condition. Extra ... This condition has an autosomal dominant pattern of inheritance, which means one copy of ...
- ... affected children are much more likely to have intellectual disability, developmental delay, and learning ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
- ... lead to problems in the urinary tract.Mild intellectual disability and developmental delay occur in about 50 percent of people with Opitz G/BBB syndrome. ...
- ... typically associated with Gorlin syndrome, including delayed development, ... the PTCH1 gene account for 50 to 85 percent of cases of Gorlin syndrome, ...
- ... and most intermediate forms are inherited in an autosomal dominant ... affected parent has a 50 percent chance of inheriting the disorder.CMT4, a ...
- ... the relationship between these brain abnormalities and the intellectual disability associated ... is unknown. About 50 affected individuals have been described in the medical ...
- ... 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 ...
- ... verbal communication. Most affected individuals also have mild intellectual disability. Their development of motor skills, such as sitting ... itself. SRCAP This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
