Journal
JOURNAL OF BONE AND MINERAL METABOLISM
Volume 32, Issue 4, Pages 351-366Publisher
SPRINGER JAPAN KK
DOI: 10.1007/s00774-013-0551-9
Keywords
Familial primary hyperparathyroidism; Multiple endocrine neoplasia type 1 and 2A; Hyperparathyroidism-jaw tumor syndrome; Familial benign hypocalciuric hypercalcemia; Familial isolated hyperparathyroidism
Ask authors/readers for more resources
Primary hyperparathyroidism is a heterogeneous clinical entity. In the clinical setting, the diagnosis and management of familial isolated hyperparathyroidism (FIHP) and other familial hyperparathyroidism (FHPT) forms continue to rely on clinical, laboratory, and histological findings, with careful examination of the family. In this article, we report a case series of FIHP in a four-generation Greek family, with no identifiable gene mutations. Clinical approach and long-term follow-up are discussed and a narrative review of the genetic basis of this entity has been performed.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available