Molecular Basis of Primary Hyperparathyroidism
2010 (English)In: World Journal of Endocrine Surgery, ISSN 0975-5039, Vol. 2, no 2, 63-70 p.Article in journal (Other academic) Published
During the past decade and a half, studies of genetic predisposition, parathyroid tumorigenesis, and molecular genetics of familialhyperparathyroid disorders have started to unveil the molecular basis of pHPT. Primary HPT is found in several distinct disorders withautosomal dominant inheritance such as in multiple endocrine neoplasia type 1 (MEN1), MEN2A, the HPT-jaw tumor syndrome (HPT-JT),familial isolated hyperparathyroidism (FIHPT), autosomal dominant mild hyperparathyroidism (ADMH), and neonatal severe HPT (NSHPT).
Place, publisher, year, edition, pages
2010. Vol. 2, no 2, 63-70 p.
Primary hyperparathyroidism, familial, multiglandular
Medical and Health Sciences
IdentifiersURN: urn:nbn:se:uu:diva-197681OAI: oai:DiVA.org:uu-197681DiVA: diva2:613780