Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications


Autoria(s): Warner, J.; Epstein, M.; Sweet, A.; Singh, D.; Burgess, J.; Stranks, S.; Hill, P.; Perry-Keene, D.; Learoyd, D.; Robinson, B.; Birdsey, P.; Mackenzie, E.; Teh, B. T.; Prins, J. B.; Cardinal, J.
Contribuinte(s)

E. R. Maher

C. Eng

Data(s)

01/03/2004

Resumo

Familial hyperparathyroidism is not uncommon in clinical endocrine practice. It encompasses a spectrum of disorders including multiple endocrine neoplasia types 1 (MEN1) and 2A, hyperparathyroidism-jaw tumour syndrome (HPT-JT), familial hypocalciuric hypercalcaemia (FHH), and familial isolated hyperparathyroidism (FIHP). Distinguishing among the five syndromes is often difficult but has profound implications for the management of patient and family. The availability of specific genetic testing for four of the syndromes has improved diagnostic accuracy and simplified family monitoring in many cases but its current cost and limited accessibility require rationalisation of its use. No gene has yet been associated exclusively with FIHP. FIHP phenotypes have been associated with mutant MEN1 and calcium-sensing receptor ( CASR) genotypes and, very recently, with mutation in the newly identified HRPT2 gene. The relative proportions of these are not yet clear. We report results of MEN1, CASR, and HRPT2 genotyping of 22 unrelated subjects with FIHP phenotypes. We found 5 (23%) with MEN1 mutations, four (18%) with CASR mutations, and none with an HRPT2 mutation. All those with mutations had multiglandular hyperparathyroidism. Of the subjects with CASR mutations, none were of the typical FHH phenotype. These findings strongly favour a recommendation for MEN1 and CASR genotyping of patients with multiglandular FIHP, irrespective of urinary calcium excretion. However, it appears that HRPT2 genotyping should be reserved for cases in which other features of the HPT-JT phenotype have occurred in the kindred. Also apparent is the need for further investigation to identify additional genes associated with FIHP.

Identificador

http://espace.library.uq.edu.au/view/UQ:70391

Idioma(s)

eng

Publicador

BMJ Publishing Group

Palavras-Chave #Genetics & Heredity #Endocrine Neoplasia Type-1 #Neonatal Severe Hyperparathyroidism #Hypocalciuric Hypercalcemia #Parathyroid Adenomas #Receptor Gene #Men1 Gene #Benign Hypercalcemia #Ret Protooncogene #Mutation Analysis #Calcium Receptor #C1 #321004 Endocrinology #730105 Endocrine organs and diseases (incl. diabetes)
Tipo

Journal Article