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Rare Presentation of Alopecia Universalis Congenita and Twenty-nail Dystrophy in Siblings
Congenital alopecia universalis is one of the rarest anomaly which involves skin and appendages. The inheritance pattern can be autosomal recessive, X-linked recessive, or autosomal dominant. However, the most common is autosomal recessive form and it is the most severe phenotype. Twenty-nail dystro...
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| Publicado no: | Int J Trichology |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5551308/ https://ncbi.nlm.nih.gov/pubmed/28839389 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijt.ijt_48_17 |
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