Condition

Neuroferritinopathy

Diseases of the Nervous System

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
Body System
Nervous System 1
ICD-10 Chapter
VI: Diseases of the Nervous System 2
Communicable or Non-communicable
Non-Communicable 1
Transmission Route
Non-Transmissible 3
First Described
2001 1
Prevalence Band
Rare (Under 1 in 2000) 4
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
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.
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2. Orphadata (Orphanet): Orphadata cross-references for ORPHA:157846 Neuroferritinopathy
Orphadata (Orphanet)ICD-10 cross-reference
Quote, 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 Inheritance
Quote, Description and Inheritance
Mutations in the FTL gene cause neuroferritinopathy.
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4. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:157846
Quote, ORPHA:157846
Point prevalence Class only <1 / 1 000 000
View the Source
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