Catalog

Motor neuron disease in hereditary spastic paraplegia

No MMS code

Link to WHO Definition

Motor neuron disease in hereditary spastic paraplegia – http://id.who.int/icd/entity/349547398

In some genetic subtypes of hereditary spastic paraplegia, patients demonstrate clinical signs or neurophysiological evidence of sensorimotor, or more rarely, pure motor neuropathy. This may make differentiation from ALS difficult.