Literature DB >> 8279493

Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly: report of a new patient with additional findings.

M Silengo1, M Lerone, G Romeo, E Calcagno, G Martucciello, V Jasonni.   

Abstract

A new ectodermal dysplasia syndrome was reported by Bork et al. in 1987 (Hautarzt 38:342-347). The syndrome consisted of hypotrichosis with the typical SEM (scanning electron microscopy) changes of uncombable hair, retinal pigmentary dystrophy, juvenile cataract, oligodontia, brachydactyly with brachymetacarpia; it was inherited as an autosomal dominant trait. We describe a sporadic case and add further clinical findings to expand the spectrum of this rare syndrome.

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Year:  1993        PMID: 8279493     DOI: 10.1002/ajmg.1320470624

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


  2 in total

1.  Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre.

Authors:  V V Smith; G Anderson; M Malone; N J Sebire
Journal:  J Clin Pathol       Date:  2005-12       Impact factor: 3.411

Review 2.  Odontomas and supernumerary teeth: is there a common origin?

Authors:  Roberto Pippi
Journal:  Int J Med Sci       Date:  2014-11-12       Impact factor: 3.738

  2 in total

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