Free Communications

17-Hydroxylase Deficiency: Rare Cause of Delayed Puberty
  • Ayla Güven
  • Tülay Güran
  • Nils Krone
J Clin Res Pediatr Endocrinol 2017; 9: 26-26

Case Report

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign
  • Emine Çamtosun
  • Zeynep Şıklar
  • Serdar Ceylaner
  • Pınar Kocaay
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2017; 9: 163-167 DOI: 10.4274/jcrpe.3839 PMID:28008861

Original Article

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations
  • Aslı Derya Kardelen
  • Güven Toksoy
  • Firdevs Baş
  • Zehra Yavaş Abalı
  • Genco Gençay
  • Şükran Poyrazoğlu
  • Rüveyde Bundak
  • Umut Altunoğlu
  • Şahin Avcı
  • Adam Najaflı
  • Oya Uyguner
  • Birsen Karaman
  • Seher Başaran
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2018; 10: 206-215 DOI: 10.4274/jcrpe.0032 PMID:29595516