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A Rare Presentation of Multiple Endocrine Neoplasia Type 1

Background: Multiple endocrine neoplasia type 1 (MEN1) is a rare, autosomal dominant inherited syndrome caused by mutations in the MEN1 tumor suppressor gene with a reported incidence of 2 in 100,000. Clinical Case: A 26-year-old Caucasian female was seen for surveillance screening given positive fa...

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Detalhes bibliográficos
Publicado no:J Endocr Soc
Main Authors: Pradeep, Pallavi, Eisenberg, Yuval
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8265614/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.2022
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