Literature DB >> 2012121

The Rapp-Hodgkin syndrome.

E J Breslau-Siderius1, A P Lavrijsen, F W Otten, J G van der Schroeff, J G Swart.   

Abstract

We report on a family with the Rapp-Hodgkin ectodermal dysplasia syndrome. Four affected family members are described and a review of the literature is given.

Entities:  

Mesh：

Year:  1991        PMID： 2012121     DOI： 10.1002/ajmg.1320380124

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


  3 in total

1.  Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?

Authors:  D Soekarman; J P Fryns
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

2.  Cephalometric analysis of Rapp-Hodgkin syndrome.

Authors:  T C Hart; S Kyrkanides
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

3.  Palmoplantar keratoderma: An unusual manifestation of hypohydrotic ectodermic dysplasia.

Authors:  Wissal Abdelli; Asmahen Souissi; Fatima Alaoui; Wiem Sassi; Ines Chelly; Slim Haouat; Mourad Mokni
Journal:  Clin Case Rep       Date:  2022-03-13
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.