Hereditær Amyloidose

Engelsk navn: Hereditary ATTR amyloidosis
Engelske synonym: Familial TTR-related amyloidosis,Familial transthyretin-related amyloidosis


A rare genetic systemic disease characterized by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement.

Fra Orphanet

ORPHA: 271861
Klassifiseringsnivå: Group of disorders

Mer informasjon

Deler av informasjonen over er hentet fra ORPHAdata med lisens: Commons Attribution 4.0 International (CC BY 4.0)