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Results 1 - 3 of 3 for Rett "syndrome," congenital variant
  1. FOXG1 syndrome 
    ... have children. FOXG1-related disorder Genetic Testing Registry: Rett syndrome, congenital variant FOXG1 syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/foxg1-syndrome - Genetics
  2. 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
  3. Beta-propeller protein-associated neurodegeneration 
    ... often compared to features of a disorder called Rett syndrome. These features include repeated hand wringing or clasping ( ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics