Cargando…
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...
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: | |
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 |
Ejemplares similares
-
A Novel Variant in Iranian Patient with Cystinuria: A Case Report
por: Mardi, Ali, et al.
Publicado: (2021) -
Bimatoprost in the Treatment of Eyelash Universalis Alopecia Areata
por: Vila, Teresa Ojeda, et al.
Publicado: (2010) -
Alopecia universalis in a patient with Sheehan's syndrome
por: Bansal, Shivani, et al.
Publicado: (2016) -
Transient Efficacy of Tofacitinib in Alopecia Areata Universalis
por: Anzengruber, Florian, et al.
Publicado: (2016) -
Improvement of atopic dermatitis and alopecia universalis with dupilumab
por: Alotaibi, Lama, et al.
Publicado: (2021)