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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Detalles Bibliográficos
Autores principales: Mazzarello, Vittorio, Ferrari, Marco, Ena, Pasquale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078079/
https://www.ncbi.nlm.nih.gov/pubmed/30122969
http://dx.doi.org/10.2147/CCID.S167942

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078079/
https://www.ncbi.nlm.nih.gov/pubmed/30122969
http://dx.doi.org/10.2147/CCID.S167942

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