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

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SAVAS-ERDEVE S., CETINKAYA S., Abali Z. Y., Poyrazoglu S., Bas F., Berberoglu M., ...More

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

• 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
• Istanbul 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.