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ADan amyloidosis

Disease definition

A rare, neurodegenerative disease characterized by progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves.

ORPHA:97346

Classification level: Subtype of disorder
  • Synonym(s):
    • Familial dementia, Danish type
  • Prevalence: -
  • Inheritance: Autosomal dominant 
  • Age of onset: -
  • ICD-10: E85.4+  I68.0*
  • OMIM: 117300
  • UMLS: C1861735
  • MeSH: C538209
  • GARD: 9169
  • MedDRA: -

Detailed information

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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.