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Results 1 - 1 of 1 for Rett "syndrome," congenital variant
  1. FOXG1 gene 
    ... abnormalities. This condition was previously described as a congenital variant of Rett syndrome, which is a similar disorder of early development. ... Renieri A. Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. J Med Genet. 2010 Jan;47(1):49- ...
    https://medlineplus.gov/genetics/gene/foxg1 - Genetics