SAT-LB302 From Urolithiasis to Genetic Testing: An Unusual Presentation of MEN-4 Syndrome

Background:Germline mutations in the CDKN1B gene are responsible for Multiple Endocrine Neoplasia Type 4 (MEN 4) syndrome (Alrezk et al. 2017). Around 20 cases have been reported to date. Here, we report on a new MEN4 family which possibly extends the phenotypic spectrum attributable to germline mut...

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Veröffentlicht in:	Journal of the Endocrine Society 2020-05, Vol.4 (Supplement_1)
Hauptverfasser:	Alamri, Bader Nasser, Palma, Laura, Andonian, Sero, Foulkes, William D, Rivera, Juan Andres
Format:	Artikel
Sprache:	eng
Schlagworte:	Tumor Biology
Online-Zugang:	Volltext
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