The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine

Glucagon receptor (GCGR) defect (Mahvash disease) is an autosomal recessive hereditary pancreatic neuroendocrine tumor (PNET) syndrome that has only been reported in adults with pancreatic α cell hyperplasia and PNETs. We describe a 7-year-old girl with persistent hyperaminoacidemia, notable for ele...

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Xehetasun bibliografikoak
Egile Nagusiak: Hong Li, Lihua Zhao, Rani Singh, J. Nina Ham, Doris O. Fadoju, Lora J.H. Bean, Yan Zhang, Yong Xu, H. Eric Xu, Michael J. Gambello
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2018-12-01
Saila:Molecular Genetics and Metabolism Reports
Sarrera elektronikoa:http://www.sciencedirect.com/science/article/pii/S2214426918300776
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