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CASE REPORT
Year : 2022  |  Volume : 13  |  Issue : 3  |  Page : 195-197

Klippel‒Feil syndrome associated with mirror movements: A rare case report


Department of General Medicine, Bhagat Phool Singh Government Medical College for Women, Khanpur Kalan, Sonipat, Haryana, India

Correspondence Address:
Dr. Ankit Chamoli
Bhagat Phool Singh Government Medical College for Women, Khanpur Kalan, Sonipat, Haryana
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/injms.injms_3_22

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Klippel‒Feil syndrome, is a congenital disorder characterized by congenital fusion of two or more cervical vertebrae. Classically, there is triad of short neck, a low posterior hairline, and a limited range of neck movements. Less than half patients present with all three classical features. The presence of other anomalies may be associated with increased morbidity so complete evaluation and further management are critical in every case. Here, we are reporting a case with all clinical triad with associated mirror movements.


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