A large family with type IV radial polydactyly

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dc.contributor.authorSeyhan A.
dc.contributor.authorAkarsu N.
dc.contributor.authorKeskin F.
dc.date.accessioned2024-07-22T08:25:48Z
dc.date.available2024-07-22T08:25:48Z
dc.date.issued1998
dc.description.abstractThis study examines one of the largest pedigrees with radial polydactyly type IV (uncomplicated polysyndactyly) comprising a total of 69 individuals, of whom 26 have been affected over six generations. Typical manifestations of the pedigree were bilateral radial and ulnar digital duplications, as well as syndactyly between the middle and ring fingers and the second and third toes. There was no craniofacial anomaly in any of the 17 cases examined physically. This observation suggests that radial polydactyly type IV and Greig craniofacial-synostosis syndrome with similar digital manifestations are clinically-distinct entities. © 1998 The British Society for Surgery of the Hand.
dc.identifier.DOI-ID10.1016/S0266-7681(98)80139-3
dc.identifier.issn17531934
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/20588
dc.language.isoEnglish
dc.publisherSAGE Publications Ltd
dc.subjectFingers
dc.subjectHand Deformities, Congenital
dc.subjectHumans
dc.subjectPedigree
dc.subjectPolydactyly
dc.subjectSyndactyly
dc.subjectToes
dc.subjectarticle
dc.subjectclinical article
dc.subjectcraniofacial malformation
dc.subjectdisease classification
dc.subjectfamily
dc.subjecthuman
dc.subjectpedigree
dc.subjectpolydactyly
dc.subjectsyndactyly
dc.titleA large family with type IV radial polydactyly
dc.typeArticle

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