Neuroferritinopathy is a genetic neurodegenerative disorder in which iron accumulates in the basal ganglia, the cerebellum and the motor cortex of the human brain. The symptoms are extrapyramidal in nature, meaning they affect the control of movement, and they progress slowly. They generally do not become apparent until adulthood. The features described for the condition include chorea, which is involuntary jerking movement, dystonia, which is sustained abnormal muscle contraction and posture, and cognitive deficits, and all of these worsen with age. The condition belongs with the disorders of brain iron accumulation, and it is recorded in the atlas as a hereditary disease of the nervous system for readers who want to understand how a single inherited disorder can produce a progressive movement disorder. This entry does not give medical advice.
Facts
Classification
ICD-10 ChapterVI: Diseases of the Nervous System 2 Communicable or Non-communicable Transmission Route First Described Prevalence Band Causative Agent
Causative Agent (category) Sources
1. Neuroferritinopathy (Wikipedia)
Lead sentence
basal ganglia, cerebellum, and motor cortex of the human brain
Lead sentence [causative-agent-category]
genetic neurodegenerative disorder
Lead
Fewer than 100 cases of neuroferritinopathy have been reported since its identification in 2001.
View the Source2. Orphadata (Orphanet): Orphadata cross-references for ORPHA:157846 Neuroferritinopathy
Orphadata (Orphanet)ICD-10 cross-referenceQuote, ICD-10 cross-reference
"Reference": "G23.0", "Source": "ICD-10"
View the Source 3. MedlinePlus Genetics (U.S. National Library of Medicine): Neuroferritinopathy - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and InheritanceQuote, Description and Inheritance
Mutations in the FTL gene cause neuroferritinopathy.
View the Source 4. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:157846Quote, ORPHA:157846
Point prevalence Class only <1 / 1 000 000
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