Literature DB >> 8863167

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

L S Chitty1, N Dennis, M Baraitser.   

Abstract

We report two families with the Witkop "tooth and nail syndrome". This term is a misnomer, as the hair was mildly involved in the original case reports and in the families reported here.

Entities:  

Mesh：

Year:  1996        PMID： 8863167      PMCID： PMC1050709          DOI： 10.1136/jmg.33.8.707

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


  12 in total

1.  A Hereditary Ectodermal Dystrophy.

Authors:  H R Clouston
Journal:  Can Med Assoc J       Date:  1929-07       Impact factor: 8.262

2.  Familial Ectodermal Defect.

Authors:  R T Brain
Journal:  Proc R Soc Med       Date:  1937-12

3.  New cases of dermoodontodysplasia?

Authors:  M Pinheiro; F P Gomes-de-Sá-Filho; N Freire-Maia
Journal:  Am J Med Genet       Date:  1990-06

4.  Trichodermodysplasia with dental alterations: an apparently new genetic ectodermal dysplasia of the tricho-odonto-onychial subgroup.

Authors:  M Pinheiro; D V Freire-Maia; E Miranda; O G Silva-Filho; N Freire-Maia
Journal:  Clin Genet       Date:  1986-04       Impact factor: 4.438

5.  The "tooth and nail" type of autosomal dominant ectodermal dysplasia.

Authors:  J S Giansanti; S M Long; J L Rankin
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1974-04

6.  Autosomal dominant ectodermal dysplasia with significant dental defects.

Authors:  T H Redpath; G B Winter
Journal:  Br Dent J       Date:  1969-02-04       Impact factor: 1.626

7.  Hereditary ectodermal dysplasia. Symptoms, inheritance patterns, differential diagnosis, management.

Authors:  R B Lowry; G C Robinson; J R Miller
Journal:  Clin Pediatr (Phila)       Date:  1966-07       Impact factor: 1.168

8.  Rapp-Hodgkin ectodermal dysplasia.

Authors:  I B Felding; L J Björklund
Journal:  Pediatr Dermatol       Date:  1990-06       Impact factor: 1.588

9.  A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?

Authors:  P D Turnpenny; D C De Silva; D W Gregory; E S Gray; J C Dean
Journal:  Clin Dysmorphol       Date:  1995-10       Impact factor: 0.816

10.  Autosomal dominant hypodontia with nail dysgenesis. Report of twenty-nine cases in six families.

Authors:  C D Hudson; C J Witkop
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1975-03
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  4 in total

1.  A nonsense mutation in MSX1 causes Witkop syndrome.

Authors:  D Jumlongras; M Bei; J M Stimson; W F Wang; S R DePalma; C E Seidman; U Felbor; R Maas; J G Seidman; B R Olsen
Journal:  Am J Hum Genet       Date:  2001-05-16       Impact factor: 11.025

2.  Madarosis: a marker of many maladies.

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

3.  Keratosis pilaris revisited: is it more than just a follicular keratosis?

Authors:  Mary Thomas; Uday Sharadchandra Khopkar
Journal:  Int J Trichology       Date:  2012-10

4.  MSX1 mutation in witkop syndrome; a case report.

Authors:  Faezeh Ghaderi; Somaye Hekmat; Reza Ghaderi; Majid Fardaei
Journal:  Iran J Med Sci       Date:  2013-06
  4 in total

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