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Results 1 - 8 of 8 for Greig cephalopolysyndactyly syndrome
  1. 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 ...
  2. ... signs and symptoms overlap significantly with those of Greig cephalopolysyndactyly syndrome (described below), so acrocallosal syndrome resulting from GLI3 ...
  3. ... 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 ...
  4. ... 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 ...
  5. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  6. Hand Injuries and Disorders (National Library of Medicine)  
    No matter how old you are or what you do for a living, you are always using your hands. When there is something wrong with them, you may not be able to ...
  7. ... syndrome are similar to another genetic condition called Greig cephalopolysyndactyly syndrome. The overlapping features, which include craniosynostosis, polydactyly, and ...
  8. ... GC, Biesecker LG. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position ...