Journals / Journal of Experimental and Clinical Medicine / 2026 / Volume: 43 Issue: 2

Surgical treatment of congenital Sprengel deformity with omovertebral bone: A case report of an 8-year-old girl

Büşra Nur Özcan(ONDOKUZ MAYIS ÜNİVERSİTESİ)0000-0002-1160-4542
Sena Kamalı(ONDOKUZ MAYIS UNIVERSITY)0000-0001-9513-8755
Bedirhan Albayrak(UNIVERSITY OF HEALTH SCIENCES, SAMSUN HEALTH RESEARCH CENTER)0000-0003-0420-226X
Altan Aksu(UNIVERSITY OF HEALTH SCIENCES, SAMSUN HEALTH RESEARCH CENTER)0000-0003-3274-1957
Ahmet Uzun(ONDOKUZ MAYIS UNIVERSITY)0000-0003-4147-3798
Pages
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Publication Date
2026-06-30
DOI
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AI Summary & Key Takeaways

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

This case underscores the mechanical significance of the omovertebral bone in Sprengel deformity and supports anatomy-guided isolated excision as an effective treatment option in carefully selected pediatric patients in whom the deformity is predominantly driven by a discrete osseous connection.

📌 3 Key Takeaways

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Objective & Hypothesis:Sprengel deformity is a rare congenital anomaly resulting from failed caudal migration of the scapula during embryonic development.
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Key Findings & Data:We report the case of an 8-year-old girl with left-sided Cavendish grade III Sprengel deformity who presented with limited shoulder elevation and a well-corticated omovertebral bone extending from the C4 spinous process to the superomedial scapular angle.
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Conclusion & Impact:This case underscores the mechanical significance of the omovertebral bone in Sprengel deformity and supports anatomy-guided isolated excision as an effective treatment option in carefully selected pediatric patients in whom the deformity is predominantly driven by a discrete osseous connection.
🔬Design:Case Report
📍Scope:Comprehensive Sample
⚙️Variables:: Sprengel deformity · omovertebral bone excision · scapulothoracic dyskinesis

Abstract

Sprengel deformity is a rare congenital anomaly resulting from failed caudal migration of the scapula during embryonic development. In selected patients, an omovertebral bone may forms a rigid osseous tether between the cervical spine and scapula, restricting scapulothoracic motion and contributing substantially to functionl impairment. We report the case of an 8-year-old girl with left-sided Cavendish grade III Sprengel deformity who presented with limited shoulder elevation and a well-corticated omovertebral bone extending from the C4 spinous process to the superomedial scapular angle. Computured tomography provided detailed visulization of the morphology, orientation, thereby facilitating precise surgical planning. The patient underwent targeted posterior excision of the osseous tether without intraoperative or postoperative complications. At the six-month follow-up, marked improvement in shoulder elevation, enhanced scapular symmetry, and excellent cosmetic and functional recovery were observed. This case underscores the mechanical significance of the omovertebral bone in Sprengel deformity and supports anatomy-guided isolated excision as an effective treatment option in carefully selected pediatric patients in whom the deformity is predominantly driven by a discrete osseous connection.

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Cite This Article

Özcan, B. N., Kamalı, S., Pirzirenli, M. E., Albayrak, B., Aksu, A., Uzun, A., Coşkun, H. S. (2026). Surgical treatment of congenital Sprengel deformity with omovertebral bone: A case report of an 8-year-old girl. Journal of Experimental and Clinical Medicine, Volume: 43 Issue: 2. https://ajindex.com/articles/1422522

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