Literature DB >> 2643072

Rapp-Hodgkin syndrome: an ectodermal dysplasia involving the teeth, hair, nails, and palate. Report of a case and review of the literature.

P J Crawford1, M J Aldred, A Clarke, M S Tso.   

Abstract

Rapp-Hodgkin syndrome is a rare form of ectodermal dysplasia involving the hair, eyes, sweat glands, nails, teeth, and palate. The case of a white girl with the condition is presented. The differential diagnosis is discussed, and the eight previously reported cases are reviewed. Another (ninth) previously reported case is considered for inclusion in the group.

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Year:  1989        PMID: 2643072     DOI: 10.1016/0030-4220(89)90302-2

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol        ISSN: 0030-4220


  4 in total

1.  Hereditary hypohidrotic ectodermal dysplasia: report of a rare case.

Authors:  Geetha Paramkusam; Venkateswarlu Meduri; Lakshmi Kavitha Nadendla; Namratha Shetty
Journal:  J Clin Diagn Res       Date:  2013-09-10

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.  Hypohidrotic ectodermal dysplasia.

Authors:  Vagish Kumar L Shanbhag
Journal:  Indian Dermatol Online J       Date:  2015 Mar-Apr

4.  Ectodermal dysplasia - A rare case report.

Authors:  Poulomi Bhakta; Bhavna Barthunia; Haritma Nigam; Pallavi Pawar
Journal:  J Family Med Prim Care       Date:  2019-09-30
  4 in total

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