Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

Ocal G., BERBEROĞLU M., ŞIKLAR Z., AYCAN Z., Hacihamdioglu B., Erdeve S. S., ...Daha Fazla

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY, cilt.28, sa.1, ss.6-11, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 28 Sayı: 1
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1016/j.jpag.2014.01.106
  • Dergi Adı: JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.6-11
  • Anahtar Kelimeler: Disorders of sex development, 46,XX karyotype, Etiology, P450 OXIDOREDUCTASE DEFICIENCY, CONSENSUS STATEMENT, MANAGEMENT, DIFFERENTIATION, EXPERIENCE, MUTATIONS, INTERSEX, DSD
  • Ankara Üniversitesi Adresli: Evet

Özet

Study Objective: The aim of our study was to determine the etiologic distribution of 46,XX disorder of sexual development (DSD) according to the new DSD classification system and to evaluate the clinical features of this DSD subgroup in our patient cohort. Participants: The evaluation criteria and clinical findings of 95 46,70C patients were described by clinical presentation, gonadal morphology, genital anatomy, associated dysmorphic features, presence during prenatal period with/without postnatal virilization, hormonal characteristics, and presence or absence of steroidogenic defects among 319 patients with DSD.