Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8691974 | World Neurosurgery | 2018 | 7 Pages |
Abstract
OLMA represents a rare subtype of heritable transthyretin amyloidosis that may present with progressive neurological decline secondary to central nervous system leptomeningeal amyloid deposition. This case identifies the c.381T>G (p.Ile127Met) TTR mutation variant as being implicated in the OLMA phenotype.
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Neurology
Authors
Francois Mathieu, Erin Morgan, Joyce So, David G. Munoz, Warren Mason, Paul Kongkham,