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 (Peer-Reviewed Journal) identifier identifier

  • Publication Type: Article / Article
  • Volume: 10 Issue: 4
  • Publication Date: 2014
  • Doi Number: 10.4183/aeb.2014.687
  • Journal Name: ACTA ENDOCRINOLOGICA-BUCHAREST
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • 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.