Journals / Fiziksel Tıp ve Rehabilitasyon Bilimleri Dergisi / 2010 / Cilt: 13 - Sayı: 1

A case with multiple hereditary exostoses

Herediter multiple ekzositozlu bir olgu sunumu

Pages
34–36
DOI
—
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AI Summary & Key Takeaways

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

In this case report, we aimed to present a case that has multiple exostoses and joint limitations due to these exostoses in the several regions of the body and results of rehabilitation.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Hereditary multıple exostoses is a disease which is charecterized by exostoses that originates from the juxta epiphysial region of the long bones.
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Key Findings & Data:The common complications are pain, joint limitation, extremity asymmetry, malingnant degeneration and neurovascular compressions.
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Conclusion & Impact:In this case report, we aimed to present a case that has multiple exostoses and joint limitations due to these exostoses in the several regions of the body and results of rehabilitation.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Hereditary multıple exostoses is a disease which is charecterized by exostoses that originates from the juxta epiphysial region of the long bones. The common complications are pain, joint limitation, extremity asymmetry, malingnant degeneration and neurovascular compressions. In this case report, we aimed to present a case that has multiple exostoses and joint limitations due to these exostoses in the several regions of the body and results of rehabilitation.

Özet

Herediter multiple ekzositoz, uzun kemiklerin jukstaepifizer bölgesinden köken alan ekzostozlarla karakterize otozomal dominant bir hastalıktır. En yaygın komplikasyonları ağrı, eklem limitasyonu, ekstremite eşitsizlikleri, malign dejenerasyon ve damar-sinir basılarıdır. Biz bu yazımızda vücudunun farklı bölgelerinde çok sayıda eksositozları ve buna bağlı eklem limitasyonları olan bir olguyu ve rehabilitasyon sonuçlarını sunmayı amaçladık.

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Cite This Article

AKBAL, A., KURTARAN, A., SELÇUK, B., KİMYON, S., AKYÜZ, M. (2010). A case with multiple hereditary exostoses. Fiziksel Tıp ve Rehabilitasyon Bilimleri Dergisi, Cilt: 13 - Sayı: 1, 34–36. https://ajindex.com/articles/214183

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References (12)

  1. Karakurt L, Yılmaz E, Varol T, Özdemir H, Serin E. Dirsekte soliter osteokondroma bağlı gelişen unlar sinir basısı: Olgu sunumu. Acta Orthop Traumatol Turc 2004;38:291-4
  2. Herring JA. Benign musculoskeletal tumors. In: Tachdian’s pediatric orthopedics. Vol. 3, 3rd ed. Philadelphia: W.B. Saunders; 2002;1901-53
  3. Franch J, Font J, Ramis A, Lafuente P, Fontecha P, Cairó J. Multiple cartilaginous exostosis in a Golden Retriever cross-bred puppy. Clinical, radiographic and backscattered scanning microscopy findings.Vet Comp Orthop Traumatol. 2005;18:189-93
  4. Stieber JR, Dormans JP.Manifestations of hereditary multiple exostoses. J Am Acad Orthop Surg. 2005;13:110-20
  5. Vanita V, Sperling K, Sandhu HS, Sandhu PS, Singh JR.Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.Genet Test Mol Biomarkers 2009;13:43-9
  6. Pannier S, Legeai-Mallet L. Hereditary multiple exostoses and enchondromatosis. Best Pract Res Clin Rheumatol 2008;22:45-54
  7. Géher P, Csauth K, Kaposi NP. Two familial cases of hereditary multiple exostoses. Orv Hetil. 2000;141:289-93
  8. Köse A, Özgün H, Aydoğan G. Herediter multiple ekzostozlu bir olgu sunumu. Jinekoloji Obstetrik Pediatri Dergisi 2005;11:19-22
  9. Ofiram E, Eylon S, Porat S.Correction of knee and ankle valgus in hereditary multiple exostoses using the Ilizarov apparatus. J Orthop Traumatol. 2008;9:11-5
  10. Mermer, MJ; Gupta, MC; Salamon, PB; Benson, DR. Thoracic vertebral body exostosis as a cause of myelopathy in a patient withhereditary multiple exostoses. J Spinal Disord Tech. 2002;15:144-8
  11. Temizöz O, Bayram ‹, Akpınar F, Etlik Ö,Güler M, Sakarya ME. Malign transformasyon gösteren osteokondromatosis olgusunda radyolojik bulgular: Tıp Araştırmaları Dergisi 2003:1:31-34
  12. Togay P, Özgönenel L. Spinal kord lezyonuna eşlik eden üç nadir sendrom: olgu sunumu. Türkiye Fiziksel Tıp Rehabilitasyon Der- gisi 2002;48(3).