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Journals / Endokrinolojide Yönelişler / 2003 / Cilt: 12 - Sayı: 3

Turner syndrome with isochromosome which was suspected after hyphophysis scanning

Hipofiz taraması sonucu saptanan izokromozomlu Turner sendromu

Mehmet KESKİN
Emre ATABEK
Zehra CEYLAN
Selim KURTOĞLU
Çetin SAATÇİ
Pages
109–110
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here we report a 11 years old girl with 46,X,i(Xq) Turner syndrome with isochromosome which was suspected after hyphophysis scanning.

📌 3 Key Takeaways

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Objective & Hypothesis:Hypophysis hormones scanning is important procedure for evaluating patients with growth failure because of underlying diseases.
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Key Findings & Data:Turner syndrome is characterized by a number of variable changes in external appearance and in internal organs.
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Conclusion & Impact:Here we report a 11 years old girl with 46,X,i(Xq) Turner syndrome with isochromosome which was suspected after hyphophysis scanning.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Hypophysis hormones scanning is important procedure for evaluating patients with growth failure because of underlying diseases. Turner syndrome is characterized by a number of variable changes in external appearance and in internal organs. Gonadal dysgenesis and short stature are two characteristic features. The syndrome is caused by the complete or partial absence of one of the X chromosomes. Here we report a 11 years old girl with 46,X,i(Xq) Turner syndrome with isochromosome which was suspected after hyphophysis scanning.

Özet

Hipofiz hormonlarının taraması, büyüme geriliği tanısı alan hastalarda altta yatan bozuklukların belirlenmesinde önemli rol oynamaktadır. Turner sendromu dış görünüş ve iç organlarda değişikliklerle karakterizedir. Gonadal disgenezi ve kısa boy iki karakteristik bulgusudur. Bu sendrom X kromozomlarının birinin tam veya kısmi yokluğu sonucu oluşmaktadır. Bu yazıda büyüme geriliği düşünülen ve yapılan hipofiz taraması sırasında FSH düzeyinin yüksek bulunması ile 46,X,i (Xq) İzokromozomlu Turner sendromu tanısı alan 11 yaşında kız olgu sunulmaktadır

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Cite This Article

KESKİN, M., ATABEK, E., CEYLAN, Z., KURTOĞLU, S., SAATÇİ, Ç. (2022). Turner syndrome with isochromosome which was suspected after hyphophysis scanning. Endokrinolojide Yönelişler, Cilt: 12 - Sayı: 3, 109–110. https://ajindex.com/articles/500893