Klippel Feil Syndrome: A Case Report

Authors

  • Dhananjoy Das Assistant Professor, Autism and Child Development Centre & Child Neurology Unit, Chattogram Maa Shishu-O-Shishu Hospital Medical College, Chattogram, Bangladesh
  • M A Chowdhury Arzu Autism and Child Development Centre & Child Neurology Unit, Chattogram Maa Shishu-O-Shishu Hospital Medical College, Chattogram, Bangladesh
  • SM Zafar Hossain Autism and Child Development Centre & Child Neurology Unit, Chattogram Maa Shishu-O-Shishu Hospital Medical College, Chattogram, Bangladesh

DOI:

https://doi.org/10.3329/cmoshmcj.v19i1.48810

Keywords:

Congenital; Fusion; Klippel-Feil syndrome; Cervical vertebrae

Abstract

Klippel-Feil Syndrome (KFS) is a complex syndrome comprises of classical clinicaltriad of short neck, limitation of head and neck movements and low posteriorhairline. This syndrome is resulting from failure of the normal segmentation ofcervical vertebra.In this present case in addition to classical clinical triad we have found short stature,scoliosis at cervico- dorsal junction and sprengel deformity of the shoulder. Wedidn’t find any association of hearing impairment, congenital heart disease andrenal abnormalities. There was no any neurological deficit and normal schoolperformance.Patient with KFS usually have good prognosis if cardiopulmonary, genitourinary,auditory problems are identified and treated early.

Chatt Maa Shi Hosp Med Coll J; Vol.19 (1); January 2020; Page 78-81

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Published

2020-08-28

How to Cite

Das, D., Arzu, M. A. C., & Hossain, S. Z. (2020). Klippel Feil Syndrome: A Case Report. Chattagram Maa-O-Shishu Hospital Medical College Journal, 19(1), 78–81. https://doi.org/10.3329/cmoshmcj.v19i1.48810

Issue

Vol. 19 No. 1 (2020)

Section

Case Reports

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