Dandy-Walker Syndrome in a Child at Rural Kelantan, Malaysia

Authors

  • Qin Jia Low MBBS (Melaka Manipal Medical College) Dabong Community Clinic 18200 Dabong, Kuala Krai, Kelantan
  • Nai Chien Huan MBBS (Monash) MRCP(UK) Labuan Hospital, Federal Territory of Labuan
  • Wei Lun Tan MBBS (Melaka Manipal Medical College) Dabong Community Clinic 18200 Dabong, Kuala Krai, Kelantan

DOI:

https://doi.org/10.51200/bjms.v12i2.902

Keywords:

Dandy-Walker syndrome, hydrocephalus, chronic headache

Abstract

Dandy-Walker syndrome is a rare congenital malformation of the brain that involves the cerebellum and the fourth ventricle. It is characterised by a classical triad of hydrocephalus, cystic dilatation of the fourth ventricle and complete or partial agenesis of the vermis. Majority of cases are diagnosed during neonatal or early infantile period. In this case report, a seven-year-old boy complained of recurrent headaches for the past one year. Physical examination was unremarkable. Examination of the fundus on the same day revealed bilateral papilloedema. His subsequent computed tomography scan of the brain done at a major district hospital demonstrated features in keeping with Dandy-Walker malformation. Our case highlighted the importance of embarking on a detailed and thorough approach when dealing with a child with chronic headache, especially in rural settings where advanced medical equipment is not readily available.

Author Biography

Qin Jia Low, MBBS (Melaka Manipal Medical College) Dabong Community Clinic 18200 Dabong, Kuala Krai, Kelantan

MBBS (Melaka Manipal Medical College) Dabong Community Clinic 18200 Dabong, Kuala Krai, Kelantan, Malaysia

Downloads

Additional Files

Published

2018-06-22

How to Cite

Low, Q. J., Huan, N. C., & Tan, W. L. (2018). Dandy-Walker Syndrome in a Child at Rural Kelantan, Malaysia. Borneo Journal of Medical Sciences (BJMS), 12(2), 41. https://doi.org/10.51200/bjms.v12i2.902
Total Views: 376 | Total Downloads: 451 | Total Downloads: 0