Concurrent Klippel-Feil Anomaly, Tethering and Dermoid Cyst Misinterpreted as Pott disease: A Case Report

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Concurrent Klippel-Feil Anomaly, Tethering and Dermoid Cyst Misinterpreted as Pott disease: A Case Report

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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Association of posterior fossa dermoid cyst and Klippel-Feil syndrome.

s on the Web American Journal of Psychiatrywww.appi.org /ajp/ajptoc.html Annals of Internal Medicinewww.acponline.org /journals/annals/annaltoc.htm Annals of Otology, Rhinology, and Laryngologywww.annals.com/ Journal of Neurosurgerywww.neurosurgery.org /journals/jneuro/summary.html Laryngoscopewww.laryngoscope.com/ Neurosurgerywww.neurosurgery.org /journals/neurosur/summ...

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A case of intracranial dermoid cyst associated with the Klippel-Feil deformity and recurrent meningitis.

D.H. is the second child of healthy parents, the elder child being normal. He was first referred to the Children's Hospital in July, 1954, at the age of 4 weeks because of diarrhoea and vomiting. This was thought to be dietetic in origin, and the only abnormal finding was the presence of the Klippel-Feil deformity, which was confirmed by radiological examination (Fig. 1). Ten months later he wa...

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The 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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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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ژورنال

عنوان ژورنال: Malaysian Orthopaedic Journal

سال: 2014

ISSN: 1985-2533

DOI: 10.5704/moj.1403.002