Hereditary Transthyretin Amyloidosis
Hereditary Transthyretin Amyloidosis
ncbi.nlm.nih.gov
Unlikely diagnosis considering my neuropathy developed in 2nd decade of life, early onset mutations such as hATTR Val30Met is rare in the U.S.
I have other strong indicators of the condition but I need to look into Mitochondrial disease, chronic Inflammatory demyelinating polyneuropathy, multifocal Motor neuropathy, and charcot marie tooth disease to see if I fit into those symptom profiles better.
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