Basal Ganglia Disease Mimicking Acute Encephalitis Syndrome Among Infants of Bodo Tribe, Assam
- PMID: 34553688
Basal Ganglia Disease Mimicking Acute Encephalitis Syndrome Among Infants of Bodo Tribe, Assam
Abstract
We conducted a review of hospital records of infants with acute encephalitis syndrome with bilateral symmetrical basal ganglia infarcts, between 2011-2015, at a single center in Assam. Thiamine (as part of multivitamin injection) was used in the treatment of 23 infants and not used in 27; Only 1 (3.7%) infant died in the former group and 20 infants (86.9%) died in the latter [RR (95% CI) 0.04 (0.006,0.29); P<0.001). Two infants on follow-up had normal development, both in the thiamine group. The study suggests the possibility of subclinical thiamine deficiency, mitochondrial diseases, or SLC19A3 gene mutation in this population.
Comment in
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Encephalitis-like Presentation in Infants of Bodo Tribe - Thiamine Deficiency or Leigh-like Disease?Indian Pediatr. 2022 Apr 15;59(4):345. Indian Pediatr. 2022. PMID: 35410976 No abstract available.
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Encephalitis-like Presentation in Infants of Bodo Tribe - Thiamine Deficiency or Leigh-like Disease?: Authors' Reply.Indian Pediatr. 2022 Apr 15;59(4):345-346. Indian Pediatr. 2022. PMID: 35410977 No abstract available.
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