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Measurement & Analysis of the Temporal Discrimination Threshold Applied to Cervical Dystonia
Published on: January 27, 2018
Delayed-onset dystonia due to perinatal asphyxia: a prospective study
1, Igor Petrović, Christine Klein
1Institute of Neurology and Psychiatry for Children and Youth, Belgrade, Serbia.
Insights
Delayed-onset dystonia is rare in children surviving perinatal asphyxial hypoxic-ischemic encephalopathy (HIE). This study found approximately 1% of HIE survivors developed this condition within 7 years.
Area of Science:
- Neurology
- Pediatrics
- Developmental Neuroscience
Background:
- Perinatal asphyxial hypoxic-ischemic encephalopathy (HIE) is a significant cause of neonatal brain injury.
- Long-term neurological sequelae in HIE survivors require ongoing investigation.
- The potential for delayed-onset movement disorders following HIE is not well-established.
Observation:
- A prospective study followed 103 infants with diagnosed perinatal asphyxial HIE for 7–13 years.
- Neurological outcomes included normal development (84.5%), mild signs (6.8%), and severe cerebral palsy (8.7%).
- One patient (approx. 1%) developed possible delayed-onset segmental dystonia starting at age 4.
Findings:
- The incidence of delayed-onset dystonia in HIE survivors appears to be approximately 1% over a 7-year period.
- The identified case involved cervical dystonia with arm progression, excluding DYT1 mutations.
- This suggests a potential, albeit rare, long-term neurological complication of HIE.
Implications:
- Early identification and monitoring of HIE survivors for late-onset neurological conditions are crucial.
- Understanding the long-term risks associated with HIE can inform clinical management and prognosis.
- Further research is needed to elucidate the mechanisms and prevalence of dystonia post-HIE.
Abstract:
The objective of this work was to establish the existence and incidence of possible delayed-onset dystonia in a cohort of infants with diagnosed perinatal asphyxial hypoxic-ischemic encephalopathy (HIE). This prospective study comprised 103 survivors of perinatal asphyxial HIE, who were regularly followed and neurologically examined in the course of 7 to 13 years after birth (median 10 years). Neurological outcome at the end of the follow-up period was normal in 87 (84.5%) patients, while in 7 (6.8%) only mild neurological signs were detected (behavioral disturbances in 3, clumsiness in 2, and hypotonia in 1 patient). Severe cerebral palsy was diagnosed in nine patients (8.7%). Only one patient was diagnosed with possible delayed-onset segmental dystonia. At the age of 4 years he developed cervical dystonia with spread to one arm in the course of 1.5 years (segmental dystonia) and then stabilized. Other known causes of dystonia, including a DYT1 mutation, were excluded. Our preliminary data suggest that over the course of at least 7 years after birth, approximately 1% of infants who survived perinatal asphyxial HIE would develop delayed-onset dystonia.
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