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., ...Daha Fazla

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.30, sa.7, ss.759-766, 2017 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 30 Sayı: 7
  • Basım Tarihi: 2017
  • Doi Numarası: 10.1515/jpem-2017-0088
  • Dergi Adı: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.759-766
  • Anahtar Kelimeler: 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 Üniversitesi Adresli: Evet

Özet

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.