Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

BACKGROUND: Kindler Syndrome (KS) is a rare genodermatosis characterized by skin fragility, skin atrophy, premature aging and poikiloderma. It is caused by mutations in the FERMT1 gene, which encodes kindlin-1, a protein involved in integrin signalling and the formation of focal adhesions. Several r...

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Bibliografski detalji
Izdano u:Orphanet J Rare Dis
Glavni autori: Guerrero-Aspizua, Sara, Conti, Claudio J., Escamez, Maria Jose, Castiglia, Daniele, Zambruno, Giovanna, Youssefian, Leila, Vahidnezhad, Hassan, Requena, Luis, Itin, Peter, Tadini, Gianluca, Yordanova, Ivelina, Martin, Ludovic, Uitto, Jouni, Has, Cristina, Del Rio, Marcela
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2019
Teme:
Research
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6657209/
https://ncbi.nlm.nih.gov/pubmed/31340837
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-019-1158-6
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