Literature DB >> 6249121

Syndactyly: frequency of specific types.

E E Castilla, J E Paz, I M Orioli-Parreiras.   

Abstract

Syndactyly without other combined limb anomalies, Poland complex, or amniotic bands, was diagnosed in 174 of 599, 109 consecutive newborn infants (3/10,000). Syndactyly was the only diagnosed anomaly in 133 cases, and it was associated with other anomalies in 41. The most common type of syndactyly was isolated syndactyly of the second and third toes (70 cases), which affected more males than females, and had a higher than expected frequency of white non-Latin-European ancestry. The second most frequent type was isolated syndactyly of the middle and ring fingers (18 cases), and the third was isolated syndactyly of the fourth and fifth toes (13 cases). Considering both isolated and syndromal cases, 66% (114/172) could be assigned to one or another of the fourth genetic categories of syndactyly described by Temtamy and McKusick [1978]. This, plus the high frequency of affected first degree relatives observed (25/434:6%), suggests that the genetic forms of syndactyly may be more common than might be suspected from the small number of pedigrees in the literature.

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Year:  1980        PMID: 6249121     DOI: 10.1002/ajmg.1320050406

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  14 in total

1.  Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

Authors:  K Bosse; R C Betz; Y A Lee; T F Wienker; A Reis; H Kleen; P Propping; S Cichon; M M Nöthen
Journal:  Am J Hum Genet       Date:  2000-06-30       Impact factor: 11.025

2.  High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16Q.

Authors:  J Becker-Follmann; A Gaa; E Baùsch; E Natt; G Scherer; O von Deimling
Journal:  Mamm Genome       Date:  1997-03       Impact factor: 2.957

3.  Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.

Authors:  Rivka Sukenik Halevy; Huan-Chieh Chien; Bo Heinz; Michael J Bamshad; Deborah A Nickerson; Martin Kircher; Nadav Ahituv
Journal:  Hum Mutat       Date:  2018-03-22       Impact factor: 4.878

Review 4.  Syndactyly: phenotypes, genetics and current classification.

Authors:  Sajid Malik
Journal:  Eur J Hum Genet       Date:  2012-02-15       Impact factor: 4.246

5.  Case report of a novel nonsyndromic unilateral syndactyly of the hand.

Authors:  Julius Matthias Weinrich; Waleed Ajabnoor; Peter Bannas
Journal:  Skeletal Radiol       Date:  2017-07-26       Impact factor: 2.199

6.  The molecular genetics of human appendicular skeleton.

Authors:  Safeer Ahmad; Muhammad Zeeshan Ali; Muhammad Muzammal; Fayaz Ahmad Mir; Muzammil Ahmad Khan
Journal:  Mol Genet Genomics       Date:  2022-07-30       Impact factor: 2.980

7.  Advances in the Molecular Genetics of Non-syndromic Syndactyly.

Authors:  Hao Deng; Ting Tan
Journal:  Curr Genomics       Date:  2015-06       Impact factor: 2.236

8.  Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.

Authors:  Limeng Dai; Dan Liu; Min Song; Xueqing Xu; Gang Xiong; Kang Yang; Kun Zhang; Hui Meng; Hong Guo; Yun Bai
Journal:  PLoS One       Date:  2014-05-01       Impact factor: 3.240

9.  Foot Syndactyly: A Clinical and Demographic Analysis.

Authors:  Jong Ho Kim; Byung Jun Kim; Sung Tack Kwon
Journal:  Arch Plast Surg       Date:  2016-11-18

10.  Genetic Overview of Syndactyly and Polydactyly.

Authors:  Humayun Ahmed; Hossein Akbari; Abdolhasan Emami; Mohammad R Akbari
Journal:  Plast Reconstr Surg Glob Open       Date:  2017-11-02
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