Movement Disorders (revue)

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Delayed‐onset dystonia due to perinatal asphyxia: A prospective study

Identifieur interne : 002F05 ( Main/Exploration ); précédent : 002F04; suivant : 002F06

Delayed‐onset dystonia due to perinatal asphyxia: A prospective study

Auteurs : Nataša Cerovac [Serbie] ; Igor Petrovi [Serbie] ; Christine Klein [Allemagne] ; Vladimir S. Kosti [Serbie]

Source :

RBID : ISTEX:F9B45D4E576E87E7BD4998B39A80CDF2FF8A0090

English descriptors

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. © 2007 Movement Disorder Society

Url:
DOI: 10.1002/mds.21747


Affiliations:


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Le document en format XML

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