Ehlers-Danlos syndrome Type VI : Case report

This case, 14 year-old male, was bom to a consanguineous parents and showed joint laxity, skin changes and kyphoscoliosis which are the characteristic features of Ehlers-Danlos syndrome type VI.

📌 3 Key Takeaways

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Objective & Hypothesis:Ehlers-Danlos is a heritable connective tissue disorder.

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Key Findings & Data:Here, a case of Ehlers-Danlos syndrome type VI is presented.

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Conclusion & Impact:This case, 14 year-old male, was bom to a consanguineous parents and showed joint laxity, skin changes and kyphoscoliosis which are the characteristic features of Ehlers-Danlos syndrome type VI.

🔬Design:Research Article

📍Scope:Comprehensive Sample

⚙️Variables:Domain Parameters

Abstract

Ehlers-Danlos is a heritable connective tissue disorder. Here, a case of Ehlers-Danlos syndrome type VI is presented. This case, 14 year-old male, was bom to a consanguineous parents and showed joint laxity, skin changes and kyphoscoliosis which are the characteristic features of Ehlers-Danlos syndrome type VI.

Özet

Ehlers-Danlos sendromu bağ dokusunun genetik geçiş gösteren bir hastalığıdır. Burada, eklem gevşekliği, deri bulguları gibi sendromun temel bulgularının yanısıra belirgin kifoskolyozunun da olması nedeniyle Ehlers-Danlos tip VI tanısı almış, anne ve babası 2. kuzen olan bir erkek olgu sunulmaktadır.

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Cite This Article

ÖZKINAY, F., YENİGÜN, A., ÇOĞULU, Ö., ÇOKER, M., GÜNDÜZ, C., SARI, G., ÖZKINAY, C. (1998). Ehlers-Danlos syndrome Type VI : Case report. Ege Tıp Dergisi, Cilt: 37 - Sayı: 1, 85–88. https://ajindex.com/articles/223209