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Published on: November 3, 2016
Disturbance of motor development: a manifestation of stroke in early childhood
R S Oliveira1, S Nobre, J Antunes
1Department of Pediatrics, Hospital São Teotónio-Centro Hospitalar Tondela Viseu, Viseu, Portugal. ritas-oliveira@hotmail.com
Insights
Pediatric stroke, though rare, requires consideration for focal neurological deficits. Methylenetetrahydrofolate reductase (MTHFR) C677T heterozygosity was identified as a potential factor in this case.
Area of Science:
- Neurology
- Pediatrics
- Genetics
Background:
- Childhood stroke is an increasingly recognized cause of significant morbidity and mortality.
- Typical presentations include acute focal neurological deficits, headache, altered consciousness, or seizures.
Observation:
- An 18-month-old male presented with motor developmental delay, gait disturbance, and right hemiparesis with left arm preference.
- Brain MRI revealed extensive old ischemic injury in the left middle cerebral artery territory, affecting the corona radiata, thalamus, internal capsule, and lenticular nucleus.
Findings:
- Causal investigation identified methylenetetrahydrofolate reductase (MTHFR) C677T heterozygosity.
- The child received physiotherapy and pediatric neurology consultation, showing favorable progress without recurrent ischemic events.
Implications:
- Pediatric stroke should be considered in cases of focal neurological deficits.
- While MTHFR C677T mutation is a prothrombotic factor, direct therapeutic intervention is not necessary in the absence of hyperhomocysteinemia.
Abstract:
Stroke has been recognised more frequently in children and represents a major cause of morbidity and mortality. It usually has an acute presentation, characterised by focal neurological signs, headache, altered state of consciousness or seizures. We report the case of an 18-month-male child with motor development disturbance, gait difficulty and preferential use of the left arm with right hemiparesis at clinical exam. Brain MRI showed an extensive damage involving corona radiata, thalamus, posterior arm of the internal capsule and left lenticular nucleus with atrophic retraction of the adjacent cerebrospinal fluid pathways, suggesting old ischaemic injury of the middle cerebral artery territory. Causal research pointed out at methyltetrahydrofolate reductase (MTHFR) C677T heterozygosity. He was referenced to physiotherapy and paediatric neurology consultation with favourable evolution and no recurrence of ischaemic events. Stroke is a relatively rare phenomenon in children; however, we have to consider it as a diagnosis in the presence of focal neurological deficits. MTHFR C677T mutation is considered a prothrombotic factor; however, in the absence of hyperhomocysteinaemia, no direct therapeutic approach is necessary.
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