Abstract | 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,XX 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. RESULTS: CONCLUSION:
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Authors | Gönül Öcal, Merih Berberoğlu, Zeynep Sıklar, Zehra Aycan, Bülent Hacıhamdioglu, Şenay Savas Erdeve, Emine Çamtosun, Pınar Kocaay, Hatice I Ruhi, Birim G Kılıç, Ajlan Tukun |
Journal | Journal of pediatric and adolescent gynecology
(J Pediatr Adolesc Gynecol)
Vol. 28
Issue 1
Pg. 6-11
(Feb 2015)
ISSN: 1873-4332 [Electronic] United States |
PMID | 25444050
(Publication Type: Journal Article)
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Copyright | Copyright © 2015 North American Society for Pediatric and Adolescent Gynecology. Published by Elsevier Inc. All rights reserved. |
Topics |
- 46, XX Disorders of Sex Development
(classification, etiology)
- Adolescent
- Adrenal Hyperplasia, Congenital
(complications, genetics)
- Chicago
- Child
- Child, Preschool
- Female
- Genitalia
(abnormalities)
- Gonadal Dysgenesis
(complications, genetics)
- Humans
- Infant
- Infant, Newborn
- Ovotesticular Disorders of Sex Development
(complications, genetics)
- Retrospective Studies
- Young Adult
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