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Multidisciplinary surgical management of Cowden syndrome: Report of a case

Cowden’s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000 patients with an incomplete penetrance and variable expressivity, characterized by alterations in a tumor suppressor gene. A 14-year-old Caucasian male patient came to the attention of the authors co...

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Dades bibliogràfiques
Publicat a:J Clin Exp Dent
Autors principals: Patini, Romeo, Staderini, Edoardo, Gallenzi, Patrizia
Format: Artigo
Idioma:Inglês
Publicat: Medicina Oral S.L. 2016
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5045699/
https://ncbi.nlm.nih.gov/pubmed/27703620
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4317/jced.52919
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