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Medical condition
Greig cephalopolysyndactyly syndrome
Patient with Greig cephalopolysyndactyly syndrome showing hypertelorism and macrocephaly.
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 abnormally wide thumb or big toe (hallux).[1]
^Biesecker, Leslie G. (2008-04-24). "The Greig cephalopolysyndactyly syndrome". Orphanet Journal of Rare Diseases. 3 (1): 10. doi:10.1186/1750-1172-3-10. ISSN 1750-1172. PMC 2397380. PMID 18435847.
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malformations. Patients with other syndromes, including Pallister-Hall syndrome and Greigcephalopolysyndactylysyndrome may also display polysyndactyly...
associated with several diseases, including Greigcephalopolysyndactylysyndrome, Pallister–Hall syndrome, preaxial polydactyly type IV, and postaxial...
He wrote numerous papers on skeletal abnormalities and Greigcephalopolysyndactylysyndrome (first described in 1926) is named after him. Over the course...
a set of characteristic physiological features which define whether a syndrome is a ciliopathy. Although ciliopathies are usually considered to involve...
the involved digits. Complex syndactyly occurs as part of a syndrome (such as Apert syndrome) and typically involves more digits than simple syndactyly...
associated with several phenotypes including Greigcephalopolysyndactylysyndrome, Pallister–Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly...