Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness-Reference-Cited by-同舟云学术

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Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness

Published:2021-09 Issue:5 Volume:96 Page:569-573
ISSN:0365-0596
Container-title:Anais Brasileiros de Dermatologia
language:en
Short-container-title:Anais Brasileiros de Dermatologia

Author:

Antoniali Daniela^ORCID,Westin Andrezza Telles^ORCID,Cruz Fernanda André Martins^ORCID,Simão João Carlos Lopes^ORCID

Publisher

Elsevier BV

Subject

Dermatology

Reference10 articles.

1. Novel KRT83 and KRT86 mutations associated with monilethrix;van Steensel;Exp Dermatol,2015

2. A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families;Ullah;Clin Exp Dermatol,2015

3. Monilethrix: A New Family with the Novel Mutation in KRT81 Gene;Ferrando;Int J Trichology,2012

4. A pratical, algorithmic approach to diagnosing hair shaft disorders;Mirmirani;Int J Dermatol,2011

5. Prognosis and management of congenital hair shaft disorders with fragility – part I;Singh;Pediatr Dermatol,2016

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