Illinois Type Amyloidosis
Educational overview only. This page summarizes publicly available health information for general understanding and awareness. It does not provide medical advice, diagnosis, or treatment. For personalized guidance or care decisions, consult a qualified healthcare professional.
📋Overview
Illinois Type Amyloidosis is a legacy eponym historically used to describe a form of hereditary amyloidosis caused by mutations in the fibrinogen A alpha-chain gene (FGA). The modern preferred term is Hereditary Fibrinogen A Alpha-Chain Amyloidosis (AFib amyloidosis). This condition is characterized by abnormal deposition of fibrinogen-derived amyloid fibrils, primarily affecting the kidneys and leading to progressive renal dysfunction.
Sections:
Additional Resources
Found an Error?
Help us keep this information accurate. If you notice any incorrect details, please submit a correction request.