Hairless Gene Nonsense Mutations in Alopecia Universalis: A Case Report

Alopecia universalis (AU) congenital, known as generalized atrichia, is a severe form of autosomal recessive alopecia that results in complete hair loss of scalp and body. Mutations in the human hairless gene (HR) are associated with the phenotype of the disease. A consanguineous couple who had a ch...

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Detalles Bibliográficos
Autores principales: Heidary, Hamed, Mardi, Ali, Mousavi, Seyyed Mohammad, Khazaie, Ghasem, Golab, Fereshteh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410955/
https://www.ncbi.nlm.nih.gov/pubmed/34540749
http://dx.doi.org/10.18502/ijph.v50i6.6429

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410955/
https://www.ncbi.nlm.nih.gov/pubmed/34540749
http://dx.doi.org/10.18502/ijph.v50i6.6429

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