Multiple endocrine neoplasia type 4: a new member of the MEN family

• Published in: Endocrine Connections Vol. 12; no. 2; pp. 1 - 11
• Main Authors: Singeisen, Hélène, Renzulli, Mariko Melanie, Pavlicek, Vojtech, Probst, Pascal, Hauswirth, Fabian, Muller, Markus K, Adamczyk, Magdalene, Weber, Achim, Kaderli, Reto Martin, Renzulli, Pietro
• Format: Journal Article
• Language: English
• Published: England Bioscientifica Ltd 01.02.2023; Bioscientifica
• Subjects: cdkn1b; multiple endocrine neoplasia type 4; parathyroid gland; pituitary gland; multiple endocrine neoplasia type 4; CDKN1B; parathyroid gland; pituitary gland

Objective Multiple endocrine neoplasia type 4 (MEN4) is caused by a CDKN1B germline mutation first described in 2006. Its estimated prevalence is less than one per million. The aim of this study was to define the disease characteristics. Methods A systematic review was performed according to the PRI...