Cerebellar Ataxia, An Unusual Neurological Manifestation of Coeliac Disease- A Case Study

Authors

  • - Md Raknuzzaman Resident, Phase B, Dept. of Neurology, BSMMU, Dhaka, Bangladesh
  • Abdul Kader Sheikh Associate Professor, Dept of Neurology, BSMMU, Dhaka, Bangladesh
  • Hasan Zhahidur Rahman Professor, Department of Neurology, BSMMU, Dhaka, Bangladesh
  • SK Mahbub Alam Associate Professor, Dept of Neurology, BSMMU, Dhaka, Bangladesh
  • Saifullah Ahthesam Resident, Phase B, Dept. of Neurology, BSMMU, Dhaka, Bangladesh
  • Kazi Jannat Ara Medical Officer, Dept of Orthopaedic Surgery, BSMMU, Dhaka, Bangladesh
  • Md Rafiqul Islam Professor, Department of Neurology, BSMMU, Dhaka, Bangladesh

DOI:

https://doi.org/10.3329/bjn.v32i1.57413

Keywords:

Coeliac disease, Ataxia, Anti TTG ab

Abstract

Coeliac disease was considered as a gluten sensitive enteropathy but now due to its wide clinical presentation is considered as multisystem autoimmune disorder. Ataxia with peripheral neuropathy is a rare manifestation of gluten sensitivity. The presence of glutenrelated immune markers in normal population however complicates the reliable diagnosis of gluten related neurological disorders and clinical improvement on gluten free diet can serve as a diagnostic tool for this disease. We report a case of sporadic progressive cerebellar ataxia with peripheral neuropathy with positive anti tissue transglutaminase (antitTG) antibodies and subtotal villous atrophy in duodenal biopsy. This case highlights an important diagnostic and therapeutic principle in management of late onset idiopathic ataxia.

Bangladesh Journal of Neuroscience 2016; Vol. 32 (1): 43-46

Downloads

Download data is not yet available.
Abstract
30
PDF
45

Downloads

Published

2016-01-31

How to Cite

Md Raknuzzaman, .-., Sheikh, A. K. ., Rahman, H. Z. ., Alam, S. M. ., Ahthesam, S. ., Ara, K. J. ., & Islam, M. R. . (2016). Cerebellar Ataxia, An Unusual Neurological Manifestation of Coeliac Disease- A Case Study. Bangladesh Journal of Neuroscience, 32(1), 43–46. https://doi.org/10.3329/bjn.v32i1.57413

Issue

Section

Case Reports