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Journal :   Research Journal of Pharmacy and Technology

Volume No. :   8

Issue No. :  8

Year :  2015

Pages :   1038-1042

ISSN Print :  0974-3618

ISSN Online :  0974-360X


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Klippel-Feil Syndrome-A Consortium of Anomalies: A Review



Address:   Prema Sivakumar
Saveetha Dental College, Chennai
*Corresponding Author
DOI No: 10.5958/0974-360X.2015.00177.8

ABSTRACT:
Klippel-Feil syndrome is a bone disorder characterized by the abnormal fusion of two or more cervical vertebrae, which is present from birth. It is an autosomal dominant congenital defect. It is characterized by the classical triad-short webbed neck, low posterior hairline, restricted head and neck movements and commonly associated with a tuft of hair at lumbosacral region and torticollis (abnormal neck position).Many aspects of this syndrome are surfacing and is not clear whether it is a separate entity or if it is a part of congenital spinal deformities. Only if the link is found between the genetic etiology and phenotypical pathoanatomy, the heterogeneity of the syndrome can be understood. This disease is linked to so many other syndromes and diseases, and the clinician must be well aware of the variations, and common associations in order to avoid a misdiagnosis.
KEYWORDS:
Klippel-Feil syndrome, vertebral synostosis, cervical vertebrae fusion, congenital vertebral anomaly, brevicollis, block vertebrae.
Cite:
Prema Sivakumar. Klippel-Feil Syndrome-A Consortium of Anomalies: A Review. Research J. Pharm. and Tech. 8(8): August, 2015; Page 1038-1042.
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