Pheochromocytoma, paragangliomas, and pituitary adenoma: An unusual association in a patient with an SDHD mutation. Case report

RATIONALE: Pituitary adenomas and paragangliomas are both rare endocrine diseases. Paragangliomas (PGL)/pheochromocytomas (PHEO) are part of an inherited syndrome in about 30% to 40% of cases. Among familial cases, mutations of the succinate dehydrogenase (SDH) subunit genes (succinate dehydrogenase...

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Bibliografiske detaljer
Udgivet i:Medicine (Baltimore)
Main Authors: Lemelin, Annie, Lapoirie, Marion, Abeillon, Juliette, Lasolle, Hélène, Giraud, Sophie, Philouze, Pierre, Ceruse, Philippe, Raverot, Gérald, Vighetto, Alain, Borson-Chazot, Françoise
Format: Artigo
Sprog:Inglês
Udgivet: Wolters Kluwer Health 2019
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6708967/
https://ncbi.nlm.nih.gov/pubmed/31348302
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000016594
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