Literature DB >> 22828468

A novel mutation in CDMP1 causes brachydactyly type C with "angel-shaped phalanx". A genotype-phenotype correlation in the mutational spectrum.

Bianca Ethel Gutiérrez-Amavizca1, Aniel Jessica Leticia Brambila-Tapia, Clara Ibet Juárez-Vázquez, Muriel Holder-Espinasse, Sylvie Manouvrier-Hanu, Fabienne Escande, Patricio Barros-Núñez.   

Abstract

Brachydactyly type C (BDC), a well-recognized autosomal dominant hand malformation, displays brachymesophalangy of the second, third, and fifth fingers, a short first metacarpal, hyperphalangy, and ulnar deviation of the index finger. An "angel-shaped phalanx" is a distinctive radiological sign that can be found in BDC and other skeletal dysplasias, such as angel-shaped phalango-epiphyseal dysplasia (ASPED), an autosomal dominant skeletal abnormality characterized by a typical angel-shaped phalanx, brachydactyly, specific radiological findings, abnormal dentition, hip dysplasia, and delayed bone age. BDC and ASPED result from mutations in the CDMP1 gene. We report here a Mexican patient with BDC and clinical features of ASPED who carries a novel mutation in CDMP1, confirming that BDC and ASPED are part of the CDMP1 mutational spectrum. Based on the large number of clinical features in common, we suggest that both anomalies are part of the same clinical spectrum. Supported by an extensive review of the literature, a possible genotype-phenotype correlation in the mutational spectrum of this gene is proposed.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

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Year:  2012        PMID: 22828468     DOI: 10.1016/j.ejmg.2012.07.004

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  4 in total

1.  Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe.

Authors:  Luitgard M Graul-Neumann; Alexandra Deichsel; Ulrike Wille; Naseebullah Kakar; Randi Koll; Christian Bassir; Jamil Ahmad; Valerie Cormier-Daire; Stefan Mundlos; Christian Kubisch; Guntram Borck; Eva Klopocki; Thomas D Mueller; Sandra C Doelken; Petra Seemann
Journal:  Eur J Hum Genet       Date:  2013-10-16       Impact factor: 4.246

2.  Novel indel Mutation in the GDF5 Gene Is Associated with Brachydactyly Type C in a Four-Generation Turkish Family.

Authors:  Z O Uyguner; M Kocaoğlu; G Toksoy; S Basaran; H Kayserili
Journal:  Mol Syndromol       Date:  2014-01-03

3.  Frameshift Mutation in a Chinese Patient with Brachydactyly Type C Involving the Third Metacarpal: A Case Report.

Authors:  Qiuya Li; Fan Bai; Shanlin Chen
Journal:  Orthop Surg       Date:  2022-07-12       Impact factor: 2.279

4.  Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1.

Authors:  Lemuel Racacho; Ashley M Byrnes; Heather MacDonald; Helen J Dranse; Sarah M Nikkel; Judith Allanson; Elisabeth Rosser; T Michael Underhill; Dennis E Bulman
Journal:  Eur J Hum Genet       Date:  2015-03-11       Impact factor: 4.246

  4 in total

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