Literature DB >> 15316967

Further delineation of the odonto-onycho-dermal dysplasia syndrome.

Hala Mégarbané1, May Haddad, Valérie Delague, Julien Renoux, Nelly Boehm, André Mégarbané.   

Abstract

We report on three boys, two brothers and their maternal cousin, presenting with dry hair, pilar keratosis, severe hypodontia, smooth tongue, onychodysplasia, and keratoderma and hyperhidrosis of palms and soles. Histology of the skin showed orthokeratotic, hyperkeratosis, hypergranulosis, and mild acanthosis in the epidermis. Scanning electron microscopic examination of the hair showed longitudinal depressions in some hair. These features are close to a rare entity: the odonto-onycho-dermal dysplasia but with some differing features. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15316967     DOI: 10.1002/ajmg.a.30188

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  5 in total

1.  WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.

Authors:  Sadia Nawaz; Joakim Klar; Muhammad Wajid; Muhammad Aslam; Muhammad Tariq; Jens Schuster; Shahid Mahmood Baig; Niklas Dahl
Journal:  Eur J Hum Genet       Date:  2009-05-27       Impact factor: 4.246

2.  WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

Authors:  Axel Bohring; Thomas Stamm; Christiane Spaich; Claudia Haase; Kerstin Spree; Ute Hehr; Mandy Hoffmann; Susanne Ledig; Saadettin Sel; Peter Wieacker; Albrecht Röpke
Journal:  Am J Hum Genet       Date:  2009-06-25       Impact factor: 11.025

3.  Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

Authors:  Lynn Adaimy; Eliane Chouery; Hala Megarbane; Salman Mroueh; Valerie Delague; Elsa Nicolas; Hanen Belguith; Philippe de Mazancourt; Andre Megarbane
Journal:  Am J Hum Genet       Date:  2007-08-09       Impact factor: 11.025

4.  Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation.

Authors:  Anne Bruun Krøigård; Ole Clemmensen; Hans Gjørup; Jens Michael Hertz; Anette Bygum
Journal:  BMC Dermatol       Date:  2016-03-10

5.  Impacted Lower Second Permanent Molars at the Ramus and Coronoid Process: A New Clinical Symptom of the WNT10A Mutation in Ectodermal Dysplasia.

Authors:  Elia Sfeir; Samia Aboujaoude
Journal:  Int J Clin Pediatr Dent       Date:  2017-02-27
  5 in total

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