HYPOPARATHYROIDISM, DEAFNESS, AND RENAL DYSPLASIA


CIVAN N. , EREM C. , COSKUN H., KOCAK M. , Nuhoglu I. , ERSOZ H. O.

ACTA ENDOCRINOLOGICA-BUCHAREST, vol.10, no.4, pp.687-692, 2014 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 10 Issue: 4
  • Publication Date: 2014
  • Doi Number: 10.4183/aeb.2014.687
  • Title of Journal : ACTA ENDOCRINOLOGICA-BUCHAREST
  • Page Numbers: pp.687-692

Abstract

Background. HDR syndrome is an autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal dysplasia caused by mutation of the GATA3 gene.