Literature DB >> 11172365

Brachydactyly type C.

R C Burgess1.   

Abstract

Brachydactyly type C is an autosomal dominant disorder with markedly variable penetrance. A patient with limited gene expression has shortening limited to the middle phalanges and the first metacarpal and an elongation of the radial side of the base of the second proximal phalanx. When completely expressed the characteristic radiographic findings are shortening of all the metacarpals, greatest in the thumb, followed by the little, ring, middle, and index fingers; brachymesophalangy (shortening of the middle phalanges); shortening of the proximal phalanges of the index and middle fingers, with the proximal phalanges of the ring and small fingers of normal length; elongation of the radial side of the base of the second proximal phalanx resulting in a trapezoidal shaped epiphysis; ulnar deviation at the second and third metacarpophalangeal joints; and hypersegmentation (extra phalanx) of the index and middle fingers. The ulnar deviation of the index and middle fingers may result in scissoring and require surgical correction. The hand deformities of 10 patients with brachydactyly type C are presented to characterize the hand abnormalities in the syndrome and its variable presentation.

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Year:  2001        PMID: 11172365     DOI: 10.1053/jhsu.2001.21534

Source DB:  PubMed          Journal:  J Hand Surg Am        ISSN: 0363-5023            Impact factor:   2.230


  2 in total

1.  Familial Brachydactyly with Variable Expression in Three Family Members.

Authors:  Ankur Singh; Rajniti Prasad; Om Prakash Mishra
Journal:  Indian J Pediatr       Date:  2018-06-14       Impact factor: 1.967

2.  A 17q24.3 duplication identified in a large Chinese family with brachydactyly-anonychia.

Authors:  Mohan Liu; Xueguang Zhang; Hongqian Liu; Ying Shen
Journal:  Mol Genet Genomic Med       Date:  2020-06-25       Impact factor: 2.183

  2 in total

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