Literature DB >> 8305765

Isolated congenital atrichia in an Omani kindred.

R K Kenue1, K S al-Dhafri.   

Abstract

Congenital atrichia may occur isolated or with associated defects. The isolated variant is especially uncommon. Sporadic and familial cases have been rarely reported. We present a large inbred kindred from Oman where 22 affected members with this disorder were found over six generations. The male-to-female ratio was 1:1.4. No associated ectodermal or other defects were noted. A typical autosomal recessive mode of inheritance was documented. Though inbreeding was high, anticipated quasidominance was observed only once.

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Year:  1994        PMID: 8305765     DOI: 10.1159/000247092

Source DB:  PubMed          Journal:  Dermatology        ISSN: 1018-8665            Impact factor:   5.366


  4 in total

1.  A gene for universal congenital alopecia maps to chromosome 8p21-22.

Authors:  M M Nöthen; S Cichon; I R Vogt; S Hemmer; R Kruse; M Knapp; T Höller; M Faiyaz ul Haque; S Haque; P Propping; M Ahmad; M Rietschel
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

2.  Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichias.

Authors:  E Sprecher; R Bergman; R Szargel; R Friedman-Birnbaum; N Cohen
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

3.  Congenital atrichia associated with nevus flammeus: A rare association.

Authors:  Ep Raj Kirit; Anchala Parthasaradhi
Journal:  Indian Dermatol Online J       Date:  2014-10

4.  Congenital atrichia associated with situs inversus and mesocardia.

Authors:  S Sacchidanand; Ms Sahana; Ravi Hiremagalore; Gs Asha
Journal:  Int J Trichology       Date:  2012-07
  4 in total

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