Hairless Gene Nonsense Mutations in Alopecia Universalis: A Case Report

• Main Authors: Hamed Heidary (Author), Ali Mardi (Author), Seyyed Mohammad Mousavi (Author), Ghasem Khazaie (Author), Fereshteh Golab (Author)
• Formato: Libro
• Publicado: Tehran University of Medical Sciences, 2021-06-01T00:00:00Z.
• Subjects: article
• Acceso en liña: Connect to this object online.

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...