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Hallervorden-Spatz Disease Learning Center

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Welcome

Hallervorden-Spatz disease is a movement disorder that is passed down through families(inherited).Most cases of Hallervorden-Spatz are due to a defect in a gene that makes a protein called pantothenate kinase 2. Patient...

Basic Info

Symptoms
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Causes
Hallervorden-Spatz usually begins in childhood. Most cases of Hallervorden-Spatz are due to a defect in a gene that m...
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Tests
A nervous system (neurological) examination will show:Abnormal postures and movementsMuscle rigidityTremorsWeaknessIf...
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Treatments
The goal of treatment is to control the symptoms. Although there is no specific treatment for Hallervorden-Spatz dise...
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Available Treatments
Drugs
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Risk Factors
  • Childhood
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Complications
Medication used to treat symptoms can cause complications. Being unable to move from the disease can lead to:Blood c...
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Prevention
Genetic counseling is appropriate in families affected by this illness. There is no known way to prevent it.
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Doctor Specialties
Call your health care provider if your child develops:Increased stiffness in the arms or legsIncreasing problems at s...
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Basic Info

Multimedia

Hallervorden-Spatz disease
Pantothenate Kinase-associated Neu...
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Childhood Health Quiz
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Hallervorden-Spatz Disease
Basal Ganglia Diseases
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Multimedia

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