Skip to main content
Top
Published in: Indian Journal of Pediatrics 1/2022

01-01-2022 | Dystonia | Correspondence

An Inherited Cause of Stroke Mimic in a Toddler

Authors: Sangeetha Yoganathan, Madhan Kumar, Lenka Sushma, Sumita Danda, Maya Thomas

Published in: Indian Journal of Pediatrics | Issue 1/2022

Login to get access

Excerpt

To the Editor: Stroke mimic is one of the common causes of neurological deficits in young children. A 2-y-old-boy born to nonconsanguineous parents presented with recurrent weakness of left upper and lower limbs alternating with right upper and lower limbs, each event lasting for 48–72 h. The child was delivered at 36 wk of gestation with a birth weight of 2130 g. He had daily episodes of abnormal twisting posture of limbs and trunk with preserved awareness from first month of age. Mild developmental delay was observed. Left eye convergent squint and right hemiplegia were observed. Possibilities of alternating hemiplegia of child (AHC), mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS) and Moyamoya syndrome were considered. Brain magnetic resonance imaging with magnetic resonance angiography and electroencephalography were normal. Next generation sequencing revealed a likely pathogenic heterozygous missense variation in the exon 17 of ATP1A3 gene (c.2440G >A; p.Asp814Asn; ENST00000545399.6) confirming the diagnosis of alternating hemiplegia of childhood-2. …
Literature
1.
go back to reference Buck BH, Akhtar N, Alrohimi A, Khan K, Shuaib A. Stroke mimics: incidence, aetiology, clinical features and treatment. Ann Med. 2021;53:420–36.CrossRef Buck BH, Akhtar N, Alrohimi A, Khan K, Shuaib A. Stroke mimics: incidence, aetiology, clinical features and treatment. Ann Med. 2021;53:420–36.CrossRef
2.
go back to reference Brashear A, Sweadner KJ, Cook JF, et al. ATP1A3-Related Neurologic Disorders. 2008 Feb 7 [Updated 2018 Feb 22]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews®. Seattle (WA): University of Washington, Seattle; 1993-2021. Available at: https://www.ncbi.nlm.nih.gov/books/NBK1115/. Accessed on 17 Jun 2021 Brashear A, Sweadner KJ, Cook JF, et al. ATP1A3-Related Neurologic Disorders. 2008 Feb 7 [Updated 2018 Feb 22]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews®. Seattle (WA): University of Washington, Seattle; 1993-2021. Available at: https://​www.​ncbi.​nlm.​nih.​gov/​books/​NBK1115/​. Accessed on 17 Jun 2021
3.
go back to reference Rosewich H, Sweney MT, DeBrosse S, et al. Research conference summary from the 2014 international task force on ATP1A3 -related disorders. Neurol Genet. 2017;3:e139.CrossRef Rosewich H, Sweney MT, DeBrosse S, et al. Research conference summary from the 2014 international task force on ATP1A3 -related disorders. Neurol Genet. 2017;3:e139.CrossRef
4.
go back to reference Samanta D. Management of alternating hemiplegia of childhood: a review. Pediatr Neurol. 2020;103:12–20.CrossRef Samanta D. Management of alternating hemiplegia of childhood: a review. Pediatr Neurol. 2020;103:12–20.CrossRef
Metadata
Title
An Inherited Cause of Stroke Mimic in a Toddler
Authors
Sangeetha Yoganathan
Madhan Kumar
Lenka Sushma
Sumita Danda
Maya Thomas
Publication date
01-01-2022
Publisher
Springer India
Published in
Indian Journal of Pediatrics / Issue 1/2022
Print ISSN: 0019-5456
Electronic ISSN: 0973-7693
DOI
https://doi.org/10.1007/s12098-021-03904-4

Other articles of this Issue 1/2022

Indian Journal of Pediatrics 1/2022 Go to the issue