Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height


Savas-Erdeve S., Cetinkaya S., Abali Z. Y. , Poyrazoglu S., Bas F., BERBEROĞLU M., ...More

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.30, no.7, pp.759-766, 2017 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 30 Issue: 7
  • Publication Date: 2017
  • Doi Number: 10.1515/jpem-2017-0088
  • Title of Journal : JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
  • Page Numbers: pp.759-766

Abstract

Background: The clinical, laboratory, genetic properties and final height of a large cohort of patients with nonclassical 21-hydroxylase deficiency (NC21OHD) in Turkey were analyzed.