Rare case of complete gonadal dysgenesis in a female patient with primary amenorrhea and a 46XY karyotype

Author:

Monolov Nurbek1,Nurbekova Ulbolsun2,Mamytova Elmira1,Unusov Abdurashid3,Osmonova Meerim3,Makambaeva Meerim3,Vityala Yethindra4ORCID,Tagaev Tugolbai5

Affiliation:

1. Department of Clinical and Morphological Disciplines Salymbekov University Bishkek Kyrgyzstan

2. Inpatient Department URFA Center of Radiology Bishkek Kyrgyzstan

3. Gynecology Department DOC University Clinic Bishkek Kyrgyzstan

4. Department of Pathology International Higher School of Medicine Bishkek Kyrgyzstan

5. Department of Hospital Internal Medicine, Occupational pathology with a course of Hematology I.K. Akhunbaev Kyrgyz State Medical Academy Bishkek Kyrgyzstan

Abstract

Key Clinical MessageA comprehensive diagnostic approach is crucial for patients with primary amenorrhea and short stature. Karyotyping and imaging studies help to detect hidden chromosomal abnormalities and anatomical differences, emphasizing their value in this context.AbstractA 16‐year‐old girl with absent menstruation and short stature. Further examination revealed constitutional stunting and primary amenorrhea. Karyotyping revealed a 46, XY chromosomal abnormality, whereas pelvic ultrasonography showed uterine hypoplasia and a unicornuate uterus with a rudimentary horn. After 11 months of therapy, she experienced menarche and improved secondary sexual characteristics.

Publisher

Wiley

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