Journals / Journal of Clinical and Analytical Medicine / 2013 / Cilt: 4 - Sayı: 3

Ensede Kitle Görünümü Oluşturan Bir Klippel Feil Sendromu Olgusu

A Case of Klippel-Feil Syndrome Causing a Mass Appearance in the Nape

Pages
236–238
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

In this paper, we presenta 14-year-old subject who referred to the orthopedics clinic concerned about theswelling and the mass in the cervical region possibly being malignant.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Klippel-Feil Syndrome is a syndrome arising from insufficiency of the normal segmentation and cleavage of the cervical vertebrae in the early weeks of fetal development, accompanied by multisystem abnormalities.
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Key Findings & Data:Klippel-Feil Syndrome is a syndrome arising from insufficiency of the normal segmentation and cleavage of the cervical vertebrae in the early weeks of fetal development, accompanied by multisystem abnormalities.
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Conclusion & Impact:In this paper, we presenta 14-year-old subject who referred to the orthopedics clinic concerned about theswelling and the mass in the cervical region possibly being malignant.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Klippel-Feil Syndrome is a syndrome arising from insufficiency of the normal segmentation and cleavage of the cervical vertebrae in the early weeks of fetal development, accompanied by multisystem abnormalities. In this paper, we presenta 14-year-old subject who referred to the orthopedics clinic concerned about theswelling and the mass in the cervical region possibly being malignant.

Özet

Klippel-Feil Sendromu fetal gelişimin erken haftalarında servikal vertebranın normal segmentasyon ve bölünmesindeki yetersizlikten kaynaklanan, multipl sistemanomalilerinin eşlik ettiği bir sendromdur. Bu yazıda 14 yaşında boyunda şişlik vekitlenin malign karakterde olma endişesi ile ortopedi kliniğine başvuran olguyusunduk.

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Cite This Article

CEYLAN, M. F., ŞAHAN, M. H., ŞİRİKÇİ, A., GÜNER, S., DÖNMEZ, F. Y. (2022). Ensede Kitle Görünümü Oluşturan Bir Klippel Feil Sendromu Olgusu. Journal of Clinical and Analytical Medicine, Cilt: 4 - Sayı: 3, 236–238. https://ajindex.com/articles/561284

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References (8)

  1. Hensinger RN, Lang JE, MacEwen GD. Klippel-Feil Syndrome; A Constellation Of Associated Anomalies. J Bone Joint Surg [Am] 1974;56(6):1246-53
  2. Nagib MG, Maxwell RE, Chou NS. Klippel-Feil Syndrome In Children: Clinical Features and Management. Child’s Nerv Syst 1985;1(5):255-63
  3. Tracy MR, Dormans JP, Kusumi K. Klippel-Feil Syndrome: Clinical Features and Current Understanding Of Etiology. Clin Orthop Relat Res 2004;424(7):183-90
  4. Mahiroğulları M, Özkan H, Yıldırım N, Çilli F, Güdemez E. Klippel-Feil Syndrome and Associated Congenital Abnormalities: Evaluation Of 23 Cases. Acta Orthop Traumatol Turc 2006;40(3): 234-9
  5. Senoglu M, Ozbag D, Gumusalan Y. Two Cases of Klippel-Feil Syndrome. International Journal of Anatomical Variations 2008; 1(1):6-7
  6. Thomsen MN, Schneider U, Weber M, Johannisson R, Niethard FU. Scoliosis and Congenital Anomalies Associated With Klippel-Feil Syndrome Types I-III. Spine 1997;22(4): 396-01
  7. Konstantinou DT, Chroni E, Constantoyiannis C, Dougenis D. Klippel-Feil Syndrome Presenting With Bilateral Thoracic Outlet Syndrome. Spine 2004;29(9):189- 92
  8. Disorders of the neck. In: Herring JA, Editor. Tachdjian’s Pediatric Orthopaedics. Vol 1. 3rd ed. Philadelphia: W. B. Saunders; 2002. p. 173-87.