Literature DB >> 24179947

Hereditary hypohidrotic ectodermal dysplasia: report of a rare case.

Geetha Paramkusam1, Venkateswarlu Meduri, Lakshmi Kavitha Nadendla, Namratha Shetty.   

Abstract

Hereditary Hypohidrotic Ectodermal Dysplasia (HHED), an X-linked, recessive, Mendelian character, is seen usually in males and it is inherited through female carriers. It is characterised by congenital dysplasia of one or more ectodermal structures and it is manifested by hypohidrosis, hypotrichosis and hypodontia. It results from abnormal morphogenesis of cutaneous and oral embryonic ectoderm. Here, we are presenting a rare case of HHED in a 19 year female with classic features of this condition.

Entities:  

Keywords:  Anodontia; Hereditary hypohidrotic ectodermal dysplasia (HHED); Hypodontia; Hypohidrosis; Hypotrichosis

Year:  2013        PMID: 24179947      PMCID: PMC3809686          DOI: 10.7860/JCDR/2013/5757.3409

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  4 in total

Review 1.  Overdenture prosthesis for oral rehabilitation of hypohidrotic ectodermal dysplasia: a case report.

Authors:  E D Bonilla; L Guerra; O Luna
Journal:  Quintessence Int       Date:  1997-10       Impact factor: 1.677

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Authors:  A Itthagarun; N M King
Journal:  Quintessence Int       Date:  1997-09       Impact factor: 1.677

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Journal:  J Prosthet Dent       Date:  1995-10       Impact factor: 3.426

Review 4.  Rapp-Hodgkin syndrome: an ectodermal dysplasia involving the teeth, hair, nails, and palate. Report of a case and review of the literature.

Authors:  P J Crawford; M J Aldred; A Clarke; M S Tso
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1989-01
  4 in total

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