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

Savas-Erdeve, Senay; Cetinkaya, Semra; Abali, Zehra; Poyrazoglu, Sukran; BAŞ, Firdevs; BERBEROĞLU, MERİH; ŞIKLAR, ZEYNEP; Korkmaz, Ozlem; Bulus, Derya; Akbas, Emine; GÜRAN, TÜLAY; BÖBER, ECE; Akin, Onur; Yilmaz, Gulay; AYCAN, ZEHRA

doi:10.1515/jpem-2017-0088

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, Scopus)

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
Ankara 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.