Literature DB >> 6499270

Weyers acrodental dysostosis in a family.

M Roubicek, J Spranger.   

Abstract

A four generation family with postaxial polydactyly of hands and feet and dental anomalies is reported. Lower and upper incisors were abnormal in shape and number. Additional findings were prominent ear anthelices, hypoplastic and dysplastic nails and mild shortness of stature. Inheritance was dominant with variable expression. It is proposed that the family presents the syndrome of acrofacial dysostosis described by Weyers in 1952. To differentiate it from other acrofacial dysostoses, we suggest naming the condition acrodental dysostosis.

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Year:  1984        PMID: 6499270     DOI: 10.1111/j.1399-0004.1984.tb01108.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

Review 1.  Role of Primary Cilia in Odontogenesis.

Authors:  M Hampl; P Cela; H L Szabo-Rogers; M Kunova Bosakova; H Dosedelova; P Krejci; M Buchtova
Journal:  J Dent Res       Date:  2017-06-12       Impact factor: 6.116

2.  A novel heterozygous deletion in the EVC2 gene causes Weyers acrofacial dysostosis.

Authors:  Xiaoqian Ye; Guangtai Song; Mingwen Fan; Lisong Shi; Ethylin Wang Jabs; Shangzhi Huang; Ruiqiang Guo; Zhuan Bian
Journal:  Hum Genet       Date:  2006-01-11       Impact factor: 4.132

3.  Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus.

Authors:  T D Howard; A E Guttmacher; W McKinnon; M Sharma; V A McKusick; E W Jabs
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

4.  Report of Two Siblings with Overlapping Features of Ellis-van Creveld and Weyers Acrodental Dysostosis.

Authors:  Devi C Shetty; Harkanwal P Singh; Prince Kumar; Chanchal Verma
Journal:  J Clin Imaging Sci       Date:  2012-04-28
  4 in total

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