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Article

Familial isolated primary hyperparathyroidism due to HRPT2 mutation.

Hormones (Athens, Greece) - 1 Jan 2000

Ghemigian Adina, Ghemigian Mircea, Popescu Irina, Vija Lavinia, Petrova Eugenia, Dumitru Nicoleta, Dumitru Ioachim

Abstract excerpt

Primary hyperparathyroidism is a common endocrine disorder that is mostly caused by solitary tumors within the parathyroid glands. Characterized by early debut and higher frequency of multiple parathyroid masses, familial forms of primary hyperparathyroidism are caused by the already known mutations of: menin (MEN1 syndrome), RET proto-oncogene (MEN2 syndrome), HRPT2-parafibromin (hyperparathyroidism-jaw tumor...

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Source

Identifiers

PMID: 24121387
DOI: 10.1007/BF03401311

Genes

MEN1
RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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