A Novel Phenotype of Germline Pathogenic Variants in MAX: Concurrence of Pheochromocytoma and Ganglioneuroma in a Chinese Family and Literature Review-Reference-Cited by-同舟云学术

A Novel Phenotype of Germline Pathogenic Variants in MAX: Concurrence of Pheochromocytoma and Ganglioneuroma in a Chinese Family and Literature Review

Published:2020-08-21 Issue: Volume:11 Page:
ISSN:1664-2392
Container-title:Frontiers in Endocrinology
language:
Short-container-title:Front. Endocrinol.

Author:

Chang Xiaoyan,Li Zelin,Ma Xiaosen,Cui Yunying,Chen Shuchun,Tong Anli

Publisher

Frontiers Media SA

Subject

Endocrinology, Diabetes and Metabolism

Reference23 articles.

1. The Myc/Max/Mad network and the transcriptional control of cell behavior;Grandori;Ann Rev Cell Develop Biol.,2000

2. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma;Comino-Méndez;Nat Genet.,2011

3. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma;Burnichon;Clin Cancer Res.,2012

4. Case report of a prolactinoma in a patient with a novel MAX mutation and bilateral pheochromocytomas;Roszko;J Endocrine Soc.,2017

5. Genetic and epigenetic differences of benign and malignant pheochromocytomas and paragangliomas (PPGLs);Khatami;Endocr Regul.,2018

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1. Genotype and clinical phenotype characteristics of MAX germline mutation–associated pheochromocytoma/paraganglioma syndrome;Frontiers in Endocrinology;2024-08-30

2. Genetic diagnosis in acromegaly and gigantism: From research to clinical practice;Best Practice & Research Clinical Endocrinology & Metabolism;2024-05

3. Bilateral Pheochromocytoma with Germline MAX Variant without Family History;Clinics and Practice;2022-05-07

4. Genetic and Clinical Profiles of Pheochromocytoma and Paraganglioma: A Single Center Study;Frontiers in Endocrinology;2020-12-11