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References OMIM Gene GeneReviews HGMD HGNC
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