TY - JOUR T1 - Recognising facial onset sensory motor neuronopathy syndrome: insight from six new cases JF - Practical Neurology JO - Pract Neurol SP - 293 LP - 297 DO - 10.1136/practneurol-2014-000984 VL - 15 IS - 4 AU - R Broad AU - P N Leigh Y1 - 2015/08/01 UR - http://pn.bmj.com/content/15/4/293.abstract N2 - Facial onset sensory and motor neuronopathy (FOSMN) was first described in 2006 as an apparently sporadic neurodegenerative disease. Thirty cases have been reported to date. We summarise six new cases, highlighting the key clinical aspects of FOSMN and how to differentiate it from motor neurone disease (amyotrophic lateral sclerosis). Typically, patients present with slowly evolving numbness of the face followed by bulbar and proximal (neck and arm) weakness. However, one of our patients presented with a motor syndrome and his abnormal blink reflex studies provided a useful diagnostic clue. This extends the spectrum of the syndrome and emphasises that FOSMN should be considered in the differential diagnosis of motor neurone disease. We discuss the pathophysiology, diagnosis, prognosis and management considerations of FOSMN. ER -