Literature DB >> 508598

Hereditary hypotrichosis. A previously undescribed syndrome.

B Bentley-Phillips, H J Grace.   

Abstract

A syndrome of hereditary hypotrichosis with an unusual natural history and clinical features was encountered in a Caucasian family of four generations with a total of twenty-four members of whom eleven were affected. The mode of inheritance was autosomal dominant with variable penetrance. The loss of hair involved the scalp, eyebrows, eyelashes and body hair, manifesting itself in the school years and progressing to almost complete baldness. There were no associated abnormalities and no sex limitation. Clinical, genetic, biochemical, mechanical, histological and immunological aspects were studied. Essential differences between this type of hereditary hypotrichosis and others previously recorded are stressed.

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Year:  1979        PMID: 508598

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  3 in total

1.  The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

Authors:  M van Steensel; F J Smith; P M Steijlen; I Kluijt; H P Stevens; A Messenger; H Kremer; M G Dunnill; C Kennedy; C S Munro; V R Doherty; J A McGrath; S P Covello; C M Coleman; J Uitto; W H McLean
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

2.  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.  A Novel Pathogenic CDH3 Variant underlying Heredity Hypotrichosis Simplex detected by Whole-Exome Sequencing (WES)-A Case Report.

Authors:  Ayat Kadhi; Lamiaa Hamie; Christel Tamer; Georges Nemer; Mazen Kurban
Journal:  Cold Spring Harb Mol Case Stud       Date:  2022-08-05
  3 in total

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