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Results 1 - 6 of 6 for Greig cephalopolysyndactyly syndrome
  1. Greig cephalopolysyndactyly syndrome 
    Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. The features of this ... is unknown. Mutations in the GLI3 gene cause Greig cephalopolysyndactyly syndrome. This gene provides instructions for making a protein ...
    https://medlineplus.gov/.../greig-cephalopolysyndactyly-syndrome - Genetics
  2. GLI3 gene 
    ... signs and symptoms overlap significantly with those of Greig cephalopolysyndactyly syndrome (described below), so acrocallosal syndrome resulting from GLI3 ...
    https://medlineplus.gov/genetics/gene/gli3 - Genetics
  3. Chromosome 7 
    ... chromosome 7 are responsible for some cases of Greig cephalopolysyndactyly syndrome, a disorder that affects development of the limbs, ... tissues and organs before birth.In some cases, Greig cephalopolysyndactyly syndrome results from a rearrangement (translocation) of genetic material ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  4. Acrocallosal syndrome 
    ... significantly with those of a similar disorder called Greig cephalopolysyndactyly syndrome (which is also caused by GLI3 gene mutations), ... 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
  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