Literature DB >> 1681656

Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.

H H Ibsen1, O J Clemmensen, F Brandrup.   

Abstract

We describe a Danish family of four generations suffering from hypotrichosis of the scalp. Age at onset was 6-17 years and almost total scalp alopecia was reached by the age of 14-21 years. No associated ectodermal defects were present. Nine of 22 persons covering four generations were affected. Growth of the scalp hair slowly decreased and was accompanied by a gradual, diffuse hair loss without regional variation. A scalp biopsy was performed, revealing a non-scarring alopecia with features of androgenetic alopecia. The pedigree was compatible with autosomal dominant inheritance.

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Year:  1991        PMID: 1681656

Source DB:  PubMed          Journal:  Acta Derm Venereol        ISSN: 0001-5555            Impact factor:   4.437


  3 in total

1.  APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex.

Authors:  Yutaka Shimomura; Dritan Agalliu; Alin Vonica; Victor Luria; Muhammad Wajid; Alessandra Baumer; Serena Belli; Lynn Petukhova; Albert Schinzel; Ali H Brivanlou; Ben A Barres; Angela M Christiano
Journal:  Nature       Date:  2010-04-15       Impact factor: 49.962

2.  A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

Authors:  R C Betz; Y A Lee; A Bygum; F Brandrup; A I Bernal; J Toribio; J I Alvarez; G M Kukuk; H H Ibsen; H B Rasmussen; T F Wienker; A Reis; P Propping; R Kruse; S Cichon; M M Nöthen
Journal:  Am J Hum Genet       Date:  2000-05-02       Impact factor: 11.025

3.  Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family.

Authors:  Khalid Al Aboud; Daifullah Al Aboud
Journal:  Dermatol Reports       Date:  2011-08-03
  3 in total

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