NAGIOS: RODERIC FUNCIONANDO

Cowden's syndrome diagnosed through oral lesions : a case report

Repositori DSpace/Manakin

dc.contributor.author	Marshall, Maureen	es
dc.contributor.author	Otero, Doris	es
dc.contributor.author	Niklander, Sven	es
dc.contributor.author	Martínez, René	es
dc.date.accessioned	2023-05-31T12:29:21Z
dc.date.available	2023-05-31T12:29:21Z
dc.date.issued	2021	es
dc.identifier.citation	Marshall, M., Otero, D., Niklander, S., & Martínez-Flores, R. (2021). Cowden's syndrome diagnosed through oral lesions: A case report. Journal of clinical and experimental dentistry, 13(11), e1162–e1166.	es
dc.identifier.uri	https://hdl.handle.net/10550/87374
dc.description.abstract	Cowden's syndrome (CS), also known as multiple hamartoma syndrome, is a rare autosomal dominant genodermatosis first described in 1963. It has a high penetrance in both sexes and variable phenotypes. Its origin is a PTEN (phosphatase and tensin homologue)	es
dc.title	Cowden's syndrome diagnosed through oral lesions : a case report	es
dc.type	journal article	es_ES
dc.subject.unesco	UNESCO:CIENCIAS MÉDICAS	es
dc.identifier.doi	10.4317/jced.58890	es
dc.type.hasVersion	VoR	es_ES
dc.identifier.url	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601691/