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Ataxia

Ataxia: Excerpt from In A Page: Pediatric Signs and Symptoms

Ataxia is due to dysfunction of the cerebellum or its connections. It can present as an acute or chronic/progressive illness. Associated signs and symptoms such as papilledema, myoclonus, and retinopathy help determine the underlying etiology.

Differential Diagnosis

    • Infectious
      –Postinfectious cerebellitis: Due to varicella, EBV, mumps, Legionella, hepatitis A
      –Encephalitis, acute disseminated encephalomyelitis (ADEM)
      –Cerebellar abscess
      –Labyrinthitis
    • Toxic/metabolic encephalopathy
      –Phenytoin, carbamazepine, antihistamines, sedatives, and ethanol
  • Posterior fossa tumor
    –Medulloblastoma, glioma
  • Opsoclonus/myoclonus syndrome: May be postinfectious or paraneoplastic (reaction most likely to neuroblastoma)
  • Friedreich ataxia: Absent DTRs, positive Babinski sign, proprioceptive sensory loss, dysarthria, cardiomyopathy, diabetes
  • Ataxia-telangiectasia
  • Miller-Fisher variant of Guillain-Barré syndrome, with areflexia, ophthalmoparesis
  • Basilar migraine
  • Postconcusssion
  • Seizure
  • Arnold-Chiari, Dandy-Walker malformation
  • Cerebellar hemorrhage or ischemia
  • Multiple sclerosis
  • Vitamin E (AVED), biotinidase deficiency
    • Metabolic disorders
      –Urea cycle disorders
      –Organic acidurias (maple syrup urine disease)
      –Carbohydrate-deficient glycoprotein syndrome
  • Sphingolipidoses (GM2, Niemann-Pick type C, metachromatic leukodystrophy, Krabbe disease)
  • Neuronal ceroid-lipofuscinosis
  • Mitochondrial disease
    –NARP, MERRF, Kearns-Sayre syndrome
  • Spinocerebellar ataxias (SCA)
  • Hartnup disease
  • Refsum disease
  • Episodic ataxia type I/II (channelopathy)
  • Celiac disease
    –Have cerebellar calcification
  • Conversion disorder

Workup and Diagnosis

  • History: Acute vs chronic, progression, episodicity, recent illness (especially varicella), ingestion of toxins or drugs, trauma, previous episode of ataxia, headaches, gait disturbance, family history of migraine or spinocerebellar ataxias
    • Physical exam
      –Skin (telangiectasias), ear, sinus examination
      –Cardiac exam, abdominal masses (for neuroblastoma)
      –Neurologic exam: Cranial nerve and cerebellar examinations, papilledema, extraocular eye movements and nystagmus, DTRs, Babinski sign, proprioceptive sense, Romberg sign
  • Labs
    –Toxicology screen
    –LP (only after neuroimaging) for infection/GBS/MS
    –HVA, VMA levels (for neuroblastoma)
    –Thoracic and abdominal MRI for neuroblastoma
    –EEG for seizures
  • Metabolic testing: Serum amino acids, vitamin E, cholesterol and subtypes, lactate, pyruvate, ammonia, α - feto protein (for ataxia telangiectasia), lysosomal enzymes, transferrin eletrophoresis
    –Electromicroscopy of lymphocytes for inclusion bodies
    –Muscle biopsy for mitochondrial disease
    • Genetic testing for Friedreich ataxia and SCA
    • Imaging: CT or MRI for mass lesion or demyelination
      –MRI is superior to CT for detection of posterior fossa

    Treatment

    • In most cases, the treatment will be supportive
    • Exogenous toxins should be stopped and removed
    • Neoplasms, abscesses, hemorrhage require neurosurgical evaluation and intervention
    • Patients with Friedreich ataxia and mitochondrial disease need cardiac evaluation
    • Miller-Fisher variant of Guillain-Barré syndrome
      –Usually has a very good prognosis
      –IV immunoglobulin or plasmaphoresis may be used
    • Opsoclonus/myoclonus syndrome
      –Treated with steroids, ACTH, or IVIG
      –Neuroblastoma needs surgical evaluation
    • ADEM: Treat with high-dose intravenous steroids
    • AVED: Treat with vitamin E
    • Biotinidase deficiency: Treat with biotinidase
    • Hartnup disease: Treat with niacin
    • Refsum disease: Dietary restriction of phytanic acid
    • Epidosic ataxia: Treat with acetazolamide

Book Source Details

  • Book Title: In A Page: Pediatric Signs and Symptoms
  • Author(s): Jonathan E. Teitelbaum, Kathleen O. Deantonis, Scott Kahan
  • Year of Publication: 2007
  • Copyright Details: In A Page: Pediatric Signs and Symptoms, Copyright © 2007 Lippincott Williams & Wilkins.

More About Cerebellar ataxia syndrome

More Medical Textbooks Online about Cerebellar ataxia syndrome

Review other book chapters online related to Cerebellar ataxia syndrome:

Medical Books Excerpts
  • ATAXIA
  • "Algorithmic Diagnosis of Symptoms and Signs" (2003)
  • Ataxia
  • "In a Page: Signs and Symptoms" (2004)
  • Ataxia
  • "In A Page: Pediatric Signs and Symptoms" (2007)
  • Ataxia
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Ataxia
  • "A Pocket Manual of Differential Diagnosis" (1999)
  • Ataxia
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Ataxia
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Ataxia
  • "Field Guide to Bedside Diagnosis" (2007)
  • Ataxia
  • "Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series" (2007)
  • Ataxia
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Ataxia
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics" (2006)
  • Ataxia
  • "Nursing: Interpreting Signs and Symptoms" (2007)
 

Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.




More About This Book:
Title: In A Page: Pediatric Signs and Symptoms
Authors: Jonathan E. Teitelbaum, Kathleen O. Deantonis, Scott Kahan
Publisher: Lippincott Williams & Wilkins
Copyright: 2007
ISBN: 1-4051-0427-9

 » Next page: Ataxia (Handbook of Signs & Symptoms (Third Edition))

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