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ARMC5Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome
Author(s) -
Guillaume Assié,
Rossella Libé,
Stéphanie Espiard,
Marthe RizkRabin,
Anne Guimier,
W. Luscap,
Olivia Barreau,
Lucile Lefèvre,
Mathilde Sibony,
Laurence Guignat,
Stéphanie Rodriguez,
Karine Perlemoine,
Fernande René-Corail,
Franck Letourneur,
Bilal Trabulsi,
A. Poussier,
Nathalie ChabbertBuffet,
Françoise BorsonChazot,
Lionel Groussin,
Xavier Bertagna,
Constantine A. Stratakis,
Bruno Ragazzon,
Jérôme Bertherat
Publication year - 2013
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1304603
Subject(s) - hyperplasia , medicine , cushing syndrome , endocrinology , mutation , pathology , biology , gene , genetics
Corticotropin-independent macronodular adrenal hyperplasia may be an incidental finding or it may be identified during evaluation for Cushing's syndrome. Reports of familial cases and the involvement of both adrenal glands suggest a genetic origin of this condition.

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