Somatic Molecular Heterogeneity in Bilateral Macronodular Adrenocortical Disease (BMAD) Differs Among the Pathological Subgroups

Bilateral macronodular adrenocortical disease (BMAD) is an uncommon cause of Cushing’s syndrome leading to bilateral macronodules. Isolated BMAD has been classified into three molecular groups: patients with ARMC5 alteration, KDM1A alteration, and patients without known genetic cause. The aim of thi...

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Veröffentlicht in:	Endocrine pathology 2024-09, Vol.35 (3), p.194-206
Hauptverfasser:	Violon, Florian, Bouys, Lucas, Vaduva, Patricia, Chansavang, Albain, Vaquier, Louis, Letourneur, Franck, Izac, Brigitte, Giannone, Gaëtan, De Murat, Daniel, Gaillard, Martin, Berthon, Annabel, Ragazzon, Bruno, Pasmant, Eric, Sibony, Mathilde, Bertherat, Jérôme
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenal Cortex Diseases - complications Adrenal Cortex Diseases - genetics Adrenal Cortex Diseases - pathology Adult Aged Armadillo Domain Proteins - genetics Chromosome 1 Endocrinology Female Genes Genetic Heterogeneity Heterozygosity Histone Demethylases - genetics Hormones Humans Hyperplasia Kinases Loss of heterozygosity Male Medicine Medicine & Public Health Middle Aged Nodules Oncology Pathology Patients Proteins Tumors
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