Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis

This study highlights the importance of searching for co-occurrence of rare monogenetic neuromuscular diseases, especially in cases in which all clinical features can be readily explained by a single gene defect.

http://link.springer.com/10.1007/s10072-020-04896-3

Source: Neurological Sciences - March 13, 2021 Category: Neurology Source Type: research