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Muir-Torre Syndrome: A Case Associated with an Infrequent Gene Mutation

Muir-Torre syndrome is a rare, autosomal dominant genodermatosis characterized by the presence of at least one sebaceous gland neoplasm, associated with an underlying visceral malignancy. Muir-Torre syndrome is believed to be a subtype of Lynch Syndrome. Affected individuals are found to have germli...

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Bibliografiska uppgifter
I publikationen:J Clin Aesthet Dermatol
Huvudupphovsmän: Grob, Alexandra, Feser, Christina, Grekin, Steven
Materialtyp: Artigo
Språk:Inglês
Publicerad: Matrix Medical Communications 2016
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Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4756873/
https://ncbi.nlm.nih.gov/pubmed/26962393
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