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Striatonigral degeneration, infantile

Orpha number ORPHA1576
Prevalence of rare diseases -
Inheritance
  • Autosomal recessive
  • Mitochondrial inheritance
Age of onset -
ICD 10 code
  • G23.2
MIM number
Synonym(s) Infantile bilateral striatal necrosis
Infantile striatonigral necrosis
Striatal degeneration, familial

Summary


An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.




The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
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