Journals / Eurasian Journal of Medicine / 2012 / Cilt: 44 - Sayı: 2

Konjenital patella sendromunu taklit eden escobar sendromu

Escobar syndrome mimicing congenital patellar syndrome

Pages
117–121
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

This case were presented as it has components of Escobar syndrome and Isolated Patellar Aplasia syndrome in same time.

📌 3 Key Takeaways

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Objective & Hypothesis:Multiple pterygium syndrome (MPS) is a syndrome that is characterized abnormal face, short length and skin pterygiums on some body legions (servical, antecubital, popliteal, interdigital and on neck).
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Key Findings & Data:It is alsocalled as Pterygium Colli syndrome, Escobar syndrome or Pterygiumsyndrome.
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Conclusion & Impact:This case were presented as it has components of Escobar syndrome and Isolated Patellar Aplasia syndrome in same time.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Multiple pterygium syndrome (MPS) is a syndrome that is characterized abnormal face, short length and skin pterygiums on some body legions (servical, antecubital, popliteal, interdigital and on neck). It is alsocalled as Pterygium Colli syndrome, Escobar syndrome or Pterygiumsyndrome. Escobar (multyple pterygium) syndrome is a rare syndrome.Intrauterin growth reterdation, abnormal face, wide-spead pterygiumsthat resulted in joint contractures, ptosis, chryptoorchidism, patellardysplasia and foot deformities are seen on this syndrome. Primarly autosomal resesive crossing are observed; also autosomal dominant andX-linked crossing. This case were presented as it has components of Escobar syndrome and Isolated Patellar Aplasia syndrome in same time.

Özet

Multipl Pterjium Sendromu anormal yüz, kısa boy, vücudun bazı yerlerinde (servikal, antekübital, popliteal, parmaklararası) deri katlantıları ile karakterize bir sendromdur. Ayrıca Pterjium Kolli Sendromu,Escobar Sendromu veya Pterjium Sendromu diye adlandırılır. Escobar (Multipl Pterjium) Sendromu nadir bir sendromdur. Bu sendromda intrauterin gelişme geriliği, anaormal yüz, kontraktürler sonuçlanan geniş-yayılımlı pterjiumlar, pitosis, kriptoorşidizm, patellar displazi ve ayak deformiteleri görülür. Primer olarak otozomal resesif geçiş olmak üzere otozomal dominant ve X kromozomuna bağlı kalıtım görülür. Bu vaka Escobar ve Konjenital Patellar Sendromun komponentlerine aynı anda sahip olduğu için sunulmaktadır.

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Cite This Article

EZİRMİK, N., CAN, C. E., YILDIZ, K. (2022). Konjenital patella sendromunu taklit eden escobar sendromu. Eurasian Journal of Medicine, Cilt: 44 - Sayı: 2, 117–121. https://ajindex.com/articles/509223

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