Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System Atrophy.

CONCLUSIONS AND CLINICAL IMPLICATIONS: While MSA and SCA may have similar presentations during early disease stages, the presence of both conditions on the list of differential diagnoses can be a diagnostic dilemma. Further analysis will aid in developing a biomarker to distinguish between the two conditions and guide proper management. PMID: 32687595 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/32687595?dopt=Abstract

Source: Neurologia i Neurochirurgia Polska - July 19, 2020 Category: Neurology Authors: Hanna Al-Shaikh R, Wernick AI, Strongosky AJ, Soto-Beasley AI, van Gerpen JA, Cheshire WP, Uitti RJ, Ross OA, Wszolek ZK Tags: Neurol Neurochir Pol Source Type: research