Klippel Feil Syndrome: A Rare Case Report
نویسندگان
چکیده
INTRODUCTION In Klippel Feil syndrome, classically there is a triad of short neck, a low posterior hairline and a limited range of neck movements especially of lateral bending. In fewer than 50% of cases have all the three elements. CASE REPORT In the present case we have found congenital Scoliosis, Sprengel deformity and there were no evidence of renal disease, congenital heart disease and neurological impairment. The present case has classical triad low posterior hairline, short neck and limited cervical range of motion. CONCLUSION A rare case of Klippel Feil Syndrome is being presented with the aim that such cases should be identified and treated at an early stage to minimize cosmetic & social stigma to her and to her parents.
منابع مشابه
Klippel-Feil syndrome: a case report.
OBJECTIVE To report the clinical presentation and peculiarity of management of Klippel-Feil syndrome (KFS) at the University of Abuja Teaching Hospital, Gwagwalada. BACKGROUND KFS is a rare pathology that has not been previously reported on in Nigeria. METHODS Case review was employed to report this pathology. RESULT This case is a 10 year old boy with KFS presenting with cosmetic blemish...
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Klippel-Feil syndrome (KFS) is characterized by the failure in segmentation of two or more vertebrae due to an abnormal division of the mesodermal somites and has been reported to be associated with cardiac and central nervous system anomalies. We report a rare occurrence of concurrent Klippel-Feil anomaly, tethering and dermoid cyst of dorsal spine masquerading Potts’ disease in an eighteen ye...
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متن کاملOne Case of Klippel-Fiel Syndrome
A case of Klippel-Feil disease with epilepsy is reported and the clinical, X-ray, EE G changes in this patient are discussed and compared with the findings in the other reports. The treatment is symptomatic.
متن کاملThe Klippel-Feil syndrome: a case report.
Short neck and fusion of cervical vertebrae are observed in several genetic conditions and well-defined syndromes. An 8-year-old boy with a short neck, low-set posterior hairline, deafness and limited neck motion was suspected of having such a condition. Clinical and radiographic examination led to the diagnosis of Klippel-Feil syndrome.
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عنوان ژورنال:
دوره 4 شماره
صفحات -
تاریخ انتشار 2014