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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Detalhes bibliográficos
Publicado no:Orphanet J Rare Dis
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha: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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