Pituitary Disease in

AIP Familial isolated pituitary adenoma GPR101 acromegaly genetics pituitary apoplexy prolactinoma

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
26 Jun 2020
Historique:
received: 10 06 2020
revised: 23 06 2020
accepted: 24 06 2020
entrez: 2 7 2020
pubmed: 2 7 2020
medline: 2 7 2020
Statut: epublish

Résumé

Clinically-relevant pituitary adenomas occur in about 1:1000 of the general population, but only about 5% occur in a known genetic or familial setting. Familial isolated pituitary adenomas (FIPA) are one of the most important inherited settings for pituitary adenomas and the most frequent genetic cause is a germline mutation in the

Identifiants

pubmed: 32604740
pii: jcm9062003
doi: 10.3390/jcm9062003
pmc: PMC7356765
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : FIRS CHU de Liège
ID : 2016-2019
Organisme : JABBS Foundation
ID : 2015-2018

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Auteurs

Ismene Bilbao Garay (I)

Department of Endocrinology, Hospital Universitario Donostia, 20014 Donostia, Euskadi, Spain.

Adrian F Daly (AF)

Department of Endocrinology, Centre Hospitalaire Universitaire de Liège, Liège Université, 4000 Liège, Belgium.

Nerea Egaña Zunzunegi (N)

Department of Endocrinology, Hospital Universitario Donostia, 20014 Donostia, Euskadi, Spain.

Albert Beckers (A)

Department of Endocrinology, Centre Hospitalaire Universitaire de Liège, Liège Université, 4000 Liège, Belgium.

Classifications MeSH