Abstract
SUMMARY: Ataxia is the principal symptom of many common neurologic diseases in childhood. Ataxias caused by dysfunction of the cerebellum occur in acute, intermittent, and progressive disorders. Most of the chronic progressive processes are secondary to degenerative and metabolic diseases. In addition, congenital malformation of the midbrain and hindbrain can also be present, with posterior fossa symptoms related to ataxia. Brain MR imaging is the most accurate imaging technique to investigate these patients, and imaging abnormalities include size, shape, and/or signal of the brain stem and/or cerebellum. Supratentorial and cord lesions are also common. This review will discuss a pattern-recognition approach to inherited cerebellar ataxia in childhood. The purpose is to provide a comprehensive discussion that ultimately could help neuroradiologists better manage this important topic in pediatric neurology.
Abbreviations
- AR
- autosomal recessive
- CAC
- cerebellar ataxia in childhood
- 4H
- hypomyelination with hypogonadotropic hypogonadism and hypodontia
- JSRD
- Joubert syndrome and related disorders
- OPHN1
- oligophrenin-1
- © 2013 American Society of Neuroradiology
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