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Clinical manifestation and genetic analysis of familial rare disease genodermatosis xeroderma pigmentosum
Xeroderma pigmentosum (XP) is a rare autosomal recessive disease characterized by hypersensitivity of the skin to ultraviolet radiation and other carcinogenic agents. This ailment is characterized by increased photosensitivity, skin xerosis, early skin aging, actinic keratosis, erythematous lesions,...
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| Publicado no: | Intractable Rare Dis Res |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8122318/ https://ncbi.nlm.nih.gov/pubmed/33996357 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2020.03143 |
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