Transthyretin-related familial amyloidosis polyneuropathy with spinal cord damage: A case report

Abstract excerpt

Transthyroxin protein-related familial amyloidosis polyneuropathy is an autosomal dominant genetic disease caused by TTR gene mutation. Peripheral and autonomic nerve damage is the main disease. With the progression of the disease, heart, lung, kidney, eye and other organs are often involved. TTR gene c.148G > A (P.Vir30met) mutation is more common among known mutations, but this type of FAP is rarely involved in...

Topics

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• Amyloid
• Amyloid Neuropathies, Familial
• Amyloidosis: Diagnosis, Treatment, Outcomes
• China
• Mutation
• Mutation, Missense
• Polyneuropathies
• Prealbumin

Identifiers and source

Literature Corpus work

fca264cb-d21e-5870-9ea9-9359c3a3feac

DOI

10.21203/rs.3.rs-3458524/v1