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GCGR-related hyperglucagonemia
rareA rare tumor of pancreas caused by mutations in the GCGR gene characterized by pancreatic alpha cell hyperplasia, pancreatic neuroendocrine tumors and markedly increased serum glucagon levels in the absence of a glucagonoma syndrome. Clinical manifestations may include abdominal pain, pancreatitis, fatigue, diarrhea, and diabetes mellitus.
- Identifiers
- MONDO:0018582 OMIM:619290Orphanet:438274
- Causal genes
- GCGR
- Also known as
- alpha-cell hyperplasia with glucagonemia · Mahvash disease · MVAH · nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumor · nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumour
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