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Journals / GORM:Gynecology Obstetrics & Reproductive Medicine / 2013 / Cilt: 19 - Sayı: 3

Artrogripozis multiplex konjenita: olgu sunumu

Arthrogryposis multiplex congenita: case report

Ayla AKTULAY
Saliha SAĞNIÇ
ÖZLEM MORALOĞLU TEKİN
Yaprak ÜSTÜN ENGİN
Elif Gül EYİ YAPAR
Leyla MOLLAMAHMUTOĞLU
Pages
180–181
DOI
—
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AI Summary & Key Takeaways

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

Here we report a case with a diagnosis of AMC not diagnosed dur- ing antenatal follow-up.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Arthrogryposis multiplex congenita (AMC), characterized by multiple congenital joint contractures due to decreased fetal movements, is a non-progressive rare syndrome.
📊
Key Findings & Data:Prevalence is determined to be 1 in 3000 deliveries.
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Conclusion & Impact:Here we report a case with a diagnosis of AMC not diagnosed dur- ing antenatal follow-up.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Arthrogryposis multiplex congenita (AMC), characterized by multiple congenital joint contractures due to decreased fetal movements, is a non-progressive rare syndrome. Prevalence is determined to be 1 in 3000 deliveries. Although it is autosomal recessively inherited, sporadic cases have also been reported. Prenatal diagnosis of AMC is difficult. Here we report a case with a diagnosis of AMC not diagnosed dur- ing antenatal follow-up.

Özet

Artrogripozis multipleks konjenita (AMC) azalmış fetal hareket- ler nedeniyle multipl konjenital eklem kontraktürleri ile karakte- rize ilerleyici olmayan oldukça nadir görülen bir hastalık grubu- dur. Prevalansı 3.000 doğumda 1 olarak tespit edilmiştir. Otozomal resesif geçişli olabileceği gibi sporadik vakalar da gösterilmiştir. Prenatal tanısı oldukça güçtür. Bu yazıda prena- tal tanı alamamış bir AMC olgusu sunulmuştur.

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Cite This Article

AKTULAY, A., SAĞNIÇ, S., TEKİN, Ö. M., ENGİN, Y. Ü., YAPAR, E. G. E., MOLLAMAHMUTOĞLU, L. (2013). Artrogripozis multiplex konjenita: olgu sunumu. GORM:Gynecology Obstetrics & Reproductive Medicine, Cilt: 19 - Sayı: 3, 180–181. https://ajindex.com/articles/227005

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