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PedAM

Pediatric Disease Annotations & Medicines




Disease hyperparathyroidism
Phenotype C0001206|acromegaly
Sentences 1
PubMedID- 23542451 The objective of this study was to describe a multiple endocrine neoplasia type 1 (men1) family characterized by primary hyperparathyroidism, in association with acromegaly because of ectopic growth hormone-releasing hormone (ghrh) secretion by a pancreatic neuroendocrine tumor in a young man and with a bronchial carcinoid in his mother.

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