Nalaganje...
Late-onset Familial Amyloidotic Polyneuropathy with Bence Jones Proteinuria and Cardiomyopathy
Familial amyloidotic polyneuropathy is a genetically determined disease characterized by deposition of an anomalous transthyretin. A high index of suspicion is needed for this multisymptomatic and lethal disease to be diagnosed. The patient was a 70-year-old male examined due to hypesthesia in the h...
Shranjeno v:
| izdano v: | J Neurosci Rural Pract |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Medknow Publications & Media Pvt Ltd
2017
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5488573/ https://ncbi.nlm.nih.gov/pubmed/28694632 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jnrp.jnrp_498_16 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|