Misdiagnosis of associated mullerian agenesis in a female with 46, XX gonadal dysgenesis: a case report and review of literature
Author:
Affiliation:
1. Department of Obstetrics and Gynaecology, ZNA Middelheim, Antwerp, Belgium
2. Department of Radiology, ZNA Middelheim, Antwerp, Belgium
3. Department of Gynaecology, University Hospital Ghent, Belgium
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology
Link
https://www.tandfonline.com/doi/pdf/10.1080/01443615.2020.1798908
Reference5 articles.
1. Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015)
2. Reduced uterine volume after induction of puberty in women with hypogonadism
3. A rare case of 46,XX gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome
4. The clandestine uterus: or how the uterus escapes detection prior to puberty
5. Misdiagnosis of Mullerian agenesis in a patient with 46, XX gonadal dysgenesis: a missed opportunity for prevention of osteoporosis
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1. Unusual combination of acute aortic dissection, Mayer-Rokitansky-Küster-Hauser syndrome, and 46,XX gonadal dysgenesis: A case report;Frontiers in Cardiovascular Medicine;2022-11-10
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