J Korean Neurol Assoc.  1997 Aug;15(4):895-899.

A case of ataxia telangiectasia

Affiliations
  • 1Department of Neurology, Seoul National University Hospital.

Abstract

Ataxia telangiectasia is an autosomal recessive disorder characterized by progressive cerebellar degeneration, cancer predisposition, immune defects, radiosensitivity and genetic instability. Ataxia telangiectasia is rare and has not been reported in Korea. We present a 9-year-old girl with early onset progressive cerebellar ataxia. Neurologic examination showed gaze apraxia, bulbar dysfunction, retained tendon reflexes and conjunctival telangiectasia. Alpha-feto protein was elevated and serum IgA was decreased. Brain MRI showed prominent cerebellar atrophy. Literatures were reviewed.


MeSH Terms

Apraxias
Ataxia Telangiectasia*
Ataxia*
Atrophy
Brain
Cerebellar Ataxia
Child
Female
Humans
Immunoglobulin A
Korea
Magnetic Resonance Imaging
Neurologic Examination
Radiation Tolerance
Reflex, Stretch
Telangiectasis
Immunoglobulin A
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