Lower motor neurone signs Flashcards
LMN signs on examination
Wasting
Fasciculation
Hypotonia
Hyporeflexia
Causes of bilateral, symmetrical, and distal LMN signs
(“Motor peripheral polyneuropathy”, or + sensory disturbance = “mixed peripheral polyneuropathy”)
DDx:
Hereditary Motor and Sensory Neuropathy (HMSN)
Paraneoplastic e.g. LEMS
Lead poisoning
Acute: GBS, Botulinum
Causes of bilateral, symmetrical and proximal LMN signs
“Proximal myopathy”
Inherited: muscular dystrophy
Inflammation: polymyositis, dermatomyositis
Endocrine: Cushing’s syndrome, acromegaly, thyrotoxicosis, osteomalacia, diabetic amyotrophy
Drugs: alcohol, statins, steroids
Malignancy: paraneoplastic
Causes of unilateral LMN signs
Isolated to single limb + no sensory signs: Old polio
Localised to group of muscles with same supply: segmental - nerve roots, plexus, peripheral - mononeuropathy
Causes of hand wasting
Anterior horn: syringomyelia, MND, polio
Roots (C8 T1): spondylosis
Brachial plexus: compression from cervical rib, avulsion (Klumpke’s palsy)
Neuropathy: generalised (HMSN), mononeuritis multiplex (DM), compressive mononeuropathy.
Muscular: disuse - RhA, distal myopathy - myotonic dystrophy.
Investigations for proximal myopathy
Bloods: DM - glucose, HbA1c Muscle damage - CK, ESR, AST, LDH Endocrine - TSH, Ca, 9am cortisol, IGF-1 Antibodies: anti-Jo-1 CXR: paraneoplastic EMG Genetic analysis Muscle biopsy
Investigations for mononeuropathy
Bloods: DM - glucose, HbA1c B12, folate Vasculitis - ESR, ANA, ANCA EMG & nerve conduction
Investigations for radiculopathy/plexopathy
MRI