About: Facial onset sensory and motor neuropathy

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Facial onset sensory and motor neuronopathy, often abbreviated FOSMN, is an extremely rare disease characterised by sensory and motor loss beginning in the face and spreading to involve an increasingly larger area including the upper arms. Details of the disease, and in particular its aetiology, are currently subject to debate, mainly because FOSMN syndrome is so rare. FOSMN was first described in four patients in 2006 and subsequently in a further six patients but so far, these ten represent the only reported cases.

Property	Value
dbo:abstract	Facial onset sensory and motor neuronopathy, often abbreviated FOSMN, is an extremely rare disease characterised by sensory and motor loss beginning in the face and spreading to involve an increasingly larger area including the upper arms. Details of the disease, and in particular its aetiology, are currently subject to debate, mainly because FOSMN syndrome is so rare. FOSMN was first described in four patients in 2006 and subsequently in a further six patients but so far, these ten represent the only reported cases. (en)
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rdfs:comment	Facial onset sensory and motor neuronopathy, often abbreviated FOSMN, is an extremely rare disease characterised by sensory and motor loss beginning in the face and spreading to involve an increasingly larger area including the upper arms. Details of the disease, and in particular its aetiology, are currently subject to debate, mainly because FOSMN syndrome is so rare. FOSMN was first described in four patients in 2006 and subsequently in a further six patients but so far, these ten represent the only reported cases. (en)
rdfs:label	Facial onset sensory and motor neuropathy (en)
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