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Werner syndrome: quantitative assessment of skin aging
BACKGROUND: Werner syndrome (WS) is a rare autosomal recessive disorder characterized by premature aging in adults. Although not sufficient to diagnose WS, persistent short stature and alteration of the dentition are among the few early signs that appear at puberty and can lead to a suspected diagno...
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| Pubblicato in: | Clin Cosmet Investig Dermatol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Dove Medical Press
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6078079/ https://ncbi.nlm.nih.gov/pubmed/30122969 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CCID.S167942 |
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