Literature DB >> 856958

Autosomal recessive hydrotic ectodermal dysplasia.

K Fried.   

Abstract

First cousins, a male and a female, with a new type of hidrotic ectodermal dysplasia are described. They were each the result of first cousin marriage from the Egyptian Karaite community. They both had partial adontia, conical peg-shaped teeth, fine hair that did not grow long, normal sweating, eversion of lips, and pronounced facial similarity. The male had cleft lip on the right side while the female had a branchial cyst on the left side of the neck. The parents of both the cases were completely normal. The patients had distinct clinical similarity to the condition described by Witkop (1965) as 'Autosomal dominant dysplasia of nails and hypodontia' but the nails were less affected and the mode of inheritance was completely different.

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Mesh:

Year:  1977        PMID: 856958      PMCID: PMC1013532          DOI: 10.1136/jmg.14.2.137

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  3 in total

1.  Congenital deafness associated with onychodystrophy.

Authors:  M FEINMESSER; S ZELIG
Journal:  Arch Otolaryngol       Date:  1961-11

2.  [Ectodermal dysplasia of the anhidrotic type; 5 new cases].

Authors:  F PERABO; J A VELASCO; A PRADER
Journal:  Helv Paediatr Acta       Date:  1956-12

3.  Hydrotic ectodermal dysplasia--Clouston's family revisited.

Authors:  M Williams; F C Fraser
Journal:  Can Med Assoc J       Date:  1967-01-07       Impact factor: 8.262

  3 in total
  5 in total

Review 1.  Hidrotic ectodermal dysplasia of hair, teeth, and nails: case reports and review.

Authors:  L S Chitty; N Dennis; M Baraitser
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

2.  A single maxillary incisor as a manifestation of an ectodermal dysplasia.

Authors:  I Buntinx; M Baraitser
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

3.  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

4.  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

5.  Madarosis: a marker of many maladies.

Authors:  Annapurna Kumar; Kaliaperumal Karthikeyan
Journal:  Int J Trichology       Date:  2012-01
  5 in total

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