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.accessioned2024-07-18T11:49:35Z
dc.date.available2024-07-18T11:49:35Z
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.
dc.identifier.issn0266-7681
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/4142
dc.language.isoEnglish
dc.publisherCHURCHILL LIVINGSTONE
dc.subjectCRANIOSYNOSTOSIS SYNDROMES
dc.subjectGREIG SYNDROME
dc.subjectGENE
dc.subjectLOCALIZATION
dc.subjectREGION
dc.subjectLOCUS
dc.subjectMAPS
dc.titleA large family with type IV radial polydactyly
dc.typeArticle

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