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GENATLAS PHENOTYPE

last update : 27-10-2011

Symbol	MRLA
Location	3p13
Name	mental retardation with language impairment and autistic features
Corresponding gene	FOXP1
Main clinical features	mild to moderate mental retardation, language impairment, and autistic feature global delay, delayed walking, and severely delayed speech development mild dysmorphic facial features, including broad forehead, hypertelorism, downslanting palpebral fissures, ptosis, short nose, broad nasal tip, and smooth philtrum
Genetic determination	autosomal dominant
Function/system disorder	mental retardation
	psychiatry disorder
Type	disease

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