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Results 1 - 10 of 11 for Central polydactyly of fingers
  1. ... have overgrowth of the skeleton, resulting in extra fingers (polydactyly) and an unusually large head size (macrocephaly). Others with these microduplications have impaired growth, leading to short fingers (brachydactyly) and short stature. Affected individuals may also ...
  2. ... rare condition characterized by certain brain abnormalities, extra fingers and toes (polydactyly), and distinctive facial features, including widely spaced eyes ( ...
  3. ... short ribs, short arms and legs, and extra fingers or toes (polydactyly). Additional features include abnormalities in one or more ... Citation on PubMed or Free article on PubMed Central Mill P, ... cause short-rib polydactyly syndromes due to abnormal ciliogenesis. Am J Hum ...
  4. ... by certain brain abnormalities, the presence of extra fingers and toes (polydactyly), and distinctive facial features, including widely spaced eyes ( ...
  5. ... including vision loss, obesity, the presence of extra fingers and/or toes (polydactyly), kidney abnormalities, and intellectual disability. More About This ...
  6. ... including vision loss, obesity, the presence of extra fingers and/or toes (polydactyly), kidney abnormalities, and intellectual disability. More About This ...
  7. ... BPP). Some affected individuals also have an extra finger or toe on one or more of their hands or feet (polydactyly).Each of the known mutations changes a single ...
  8. ... structure. Some affected individuals also have an extra finger or toe on one or more of their hands or feet (polydactyly).Each of the known mutations changes a single ...
  9. ... Citation on PubMed or Free article on PubMed Central Howard TD, Guttmacher AE, McKinnon W, Sharma M, McKusick VA, Jabs EW. Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome ...
  10. ... Citation on PubMed or Free article on PubMed Central Okamoto T, Nagaya K, Kawata Y, Asai H, Tsuchida E, Nohara F, Okajima K, Azuma H. Novel compound heterozygous mutations in DYNC2H1 in a patient with severe short-rib polydactyly syndrome type III phenotype. Congenit Anom (Kyoto). 2015 ...
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