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Results 1 - 6 of 6 for Greig cephalopolysyndactyly "syndrome," severe
Did you mean greg cephalopolysyndactyly "syndrome," severe?
  1. Acrocallosal syndrome 
    ... and symptoms of the condition.Acrocallosal syndrome (or severe Greig cephalopolysyndactyly syndrome) resulting from GLI3 gene mutations is considered autosomal ...
    https://medlineplus.gov/genetics/condition/acrocallosal-syndrome - Genetics
  2. Chromosome 7 
    ... loss of multiple genes can cause a more severe form of this disorder called Greig cephalopolysyndactyly contiguous gene deletion syndrome. In addition to the characteristic features of the ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  3. GLI3 gene 
    ... signs and symptoms overlap significantly with those of Greig cephalopolysyndactyly syndrome (described below), so acrocallosal syndrome resulting from GLI3 gene mutations is sometimes considered a severe form of that condition.The GLI3 gene mutations ...
    https://medlineplus.gov/genetics/gene/gli3 - Genetics
  4. Greig cephalopolysyndactyly syndrome 
    Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. The features of this syndrome are highly variable, ranging from very mild to severe. People with this condition typically have one or more extra fingers or toes (polydactyly) or an ...
    https://medlineplus.gov/.../greig-cephalopolysyndactyly-syndrome - Genetics
  5. Carpenter syndrome 
    ... syndrome are similar to another genetic condition called Greig cephalopolysyndactyly syndrome. The overlapping features, which include craniosynostosis, polydactyly, and ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  6. Pallister-Hall syndrome 
    ... GC, Biesecker LG. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position ...
    https://medlineplus.gov/genetics/condition/pallister-hall-syndrome - Genetics