We present this case report as a result of chromosomal analysis (45XO/46XY) who admitted to our clinic with primary amenorrhea.
📌 3 Key Takeaways
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Objective & Hypothesis:Turner syndrome is a rare chromosomal abnormality of 45XO/46 XY mosaicism.
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Key Findings & Data:Approximately 1/10000 are seen with a phenotypic reflection of mosaicism that shows variability from a normal man to Ullrich-Turner syndrome.
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Conclusion & Impact:We present this case report as a result of chromosomal analysis (45XO/46XY) who admitted to our clinic with primary amenorrhea.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Turner syndrome is a rare chromosomal abnormality of 45XO/46 XY mosaicism. Approximately 1/10000 are seen with a phenotypic reflection of mosaicism that shows variability from a normal man to Ullrich-Turner syndrome. We present this case report as a result of chromosomal analysis (45XO/46XY) who admitted to our clinic with primary amenorrhea.
Özet
Turner sendromlu 45XO/46XY mozaikliği, nadir görülen kromozomal bir anomalidir. Yaklaşık 1/10.000 de bir görülen bu mozaismin fenotip yansımaları normal bir erkekten, klasik Ullrich-Turner Sendromuna (UTS) kadar değişen çeşitliliktedir. Primer amenore şikayeti ile kliniğimize başvuran hastanın yapılan kromozom analiz sonucu 45XO/46XY olarak geldi.
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Cite This Article
GÜNGÖREN, A., KARATEKE, A., BALOĞLU, A., HAKVERDİ, A. U., BENK, D. Ş., TERTEMİZ, S., DOLAPÇIOĞLU, S. K. (2022). A rare cause of ullrich turner syndrome of hypergonadotropic hypogonadism: A case report. Kartal Eğitim ve Araştırma Hastanesi Tıp Dergisi, Cilt: 25 - Sayı: 3, 239–241. https://ajindex.com/articles/571379
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