Literature DB >> 517571

Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: I. Affected females.

M Pinheiro, N Freire-Maia.   

Abstract

A total of 27 women of a Brazilian kindred are described as having one or more signs of the Christ-Siemens-Touraine syndrome. The history and physical examination were supplemented by four sweat tests and dermatolglyphic analysis. It is suggested that this syndrome has two forms -- a major form (in males) and a minor one (in females). Two signs verified in some of our patients (mosaic patchy distribution of body hair and radial deviation of distal phalanges of index fingers) seem to be here described for the first time. A review of the literature shows a corrected sex ratio between 1 M: 1.21 F and 1 M: 2.38 F among affecteds. Since the manifestation rate of the gene among carriers was estimated at about 0.70, the actual sex ratio is expected to be not lower than 1 M: 1.40 F. Contrary to a general opinion, affected females outnumber affected males.

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Year:  1979        PMID: 517571     DOI: 10.1002/ajmg.1320040202

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


  12 in total

1.  Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography.

Authors:  R P Clark; M R Goff; K D MacDermot
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

2.  Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations.

Authors:  A W Monreal; J Zonana; B Ferguson
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

3.  Molecular and therapeutic characterization of anti-ectodysplasin A receptor (EDAR) agonist monoclonal antibodies.

Authors:  Christine Kowalczyk; Nathalie Dunkel; Laure Willen; Margret L Casal; Elizabeth A Mauldin; Olivier Gaide; Aubry Tardivel; Giovanna Badic; Anne-Lise Etter; Manuel Favre; Douglas M Jefferson; Denis J Headon; Stéphane Demotz; Pascal Schneider
Journal:  J Biol Chem       Date:  2011-07-05       Impact factor: 5.157

4.  Hypohidrotic ectodermal dysplasia. Clinical study of a family of 30 over three generations.

Authors:  S Gilgenkrantz; C Blanchet-Bardon; V Nazzaro; L Formiga; P Mujica; Y Alembik
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

5.  Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).

Authors:  K D MacDermot; R M Winter; S Malcolm
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

6.  Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12.

Authors:  S Kølvraa; T A Kruse; P K Jensen; K H Linde; S R Vestergaard; L Bolund
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

7.  A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia.

Authors:  J A Spfaer
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

8.  Christ-Siemens-Touraine syndrome. Investigations on two large Brazilian kindreds with a new estimate of the manifestation rate among carriers.

Authors:  M Pinheiro; M T Ideriha; E A Chautard-Freire-Maia; N Freire-Maia; S L Primo-Parmo
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Generation and characterization of function-blocking anti-ectodysplasin A (EDA) monoclonal antibodies that induce ectodermal dysplasia.

Authors:  Christine Kowalczyk-Quintas; Laure Willen; Anh Thu Dang; Heidi Sarrasin; Aubry Tardivel; Katharina Hermes; Holm Schneider; Olivier Gaide; Olivier Donzé; Neil Kirby; Denis J Headon; Pascal Schneider
Journal:  J Biol Chem       Date:  2014-01-03       Impact factor: 5.157

10.  Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasia.

Authors:  A Clarke; J Burn
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

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