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What is Neuroferritinopathy (adult-onset basal ganglia disease)?

What is Neuroferritinopathy (adult-onset basal ganglia disease)?

  • Neuroferritinopathy (adult-onset basal ganglia disease): A rare disorder where a genetic mutation results in a neurological disease resulting from abnormal iron and ferritin deposits in the brain.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Neuroferritinopathy (adult-onset basal ganglia disease) as a "rare disease".
Source - Orphanet

Neuroferritinopathy (adult-onset basal ganglia disease): Introduction

Types of Neuroferritinopathy (adult-onset basal ganglia disease):

Broader types of Neuroferritinopathy (adult-onset basal ganglia disease):

What causes Neuroferritinopathy (adult-onset basal ganglia disease)?

Causes of Neuroferritinopathy (adult-onset basal ganglia disease): see causes of Neuroferritinopathy (adult-onset basal ganglia disease)

What are the symptoms of Neuroferritinopathy (adult-onset basal ganglia disease)?

Symptoms of Neuroferritinopathy (adult-onset basal ganglia disease): see symptoms of Neuroferritinopathy (adult-onset basal ganglia disease)

Onset of Neuroferritinopathy (adult-onset basal ganglia disease): Symptoms develop between the 3rd and 6th decade of life.

Neuroferritinopathy (adult-onset basal ganglia disease): Testing

Diagnostic testing: see tests for Neuroferritinopathy (adult-onset basal ganglia disease).

Misdiagnosis: see misdiagnosis and Neuroferritinopathy (adult-onset basal ganglia disease).

How is it treated?

Treatments for Neuroferritinopathy (adult-onset basal ganglia disease): see treatments for Neuroferritinopathy (adult-onset basal ganglia disease)

Name of Neuroferritinopathy (adult-onset basal ganglia disease)

Main name of condition: Neuroferritinopathy (adult-onset basal ganglia disease)

 

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