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


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

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

  • Publication Type: Article / Article
  • Volume: 30 Issue: 7
  • Publication Date: 2017
  • Doi Number: 10.1515/jpem-2017-0088
  • Journal Name: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.759-766
  • Keywords: final height, 21 hydroxylase deficiency, nonclassical congenital adrenal hyperplasia, CONGENITAL ADRENAL-HYPERPLASIA, STEROID 21-HYDROXYLASE, PUBERTAL CHANGES, ADULT HEIGHT, GENOTYPE, CORTISOL, SPECTRUM, CHILDREN, PATTERN, COHORT
  • Dokuz Eylül University Affiliated: Yes

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.