Neuromuscular Disorders Flashcards
What are the 3 clinical signs that you will always see with a neuromuscular disorder?
Reduced to absent reflexes
Muscle atrophy
Reduced muscle tone
What are some other clinical signs of neuromuscular disease?
Tetraparesis Stiff stilted gait and bunny hopping Exercise intolerance and collapse Proprioceptive deficits Muscle atrophy and tremors Ventroflexion of the head and neck
How can a neuropathy be distinguished?
Generalised or focal
Neurogenic atrophy
Severe flaccid paralysis
Sensory deficits and motor deficits
How can a junctionopathy be distinguished?
Always generalised
Exercise intolerance with fatigue
Normal sensory function
Intact reflexes
How can you distinguish a myopathy?
Generalised, symmetrical or focal Myotonia Contractures Myalgia Reduced or absent reflexes
What is the presentation of polyradiculoneuritis?
Inflammation of the nerve roots - idiopathic / rabies vaccine
Bengal cat
Acute onset, rapidly progressive pure motor deficits
Non-ambulatory tetraparesis
How can you diagnoses polyradiculoneuritis?
History and clinical signs
F waves
CSF analysis - increased protein
What is the prognosis and how can this disease be managed?
Fair
Supportive care
Turn q 4-6 h
Physiotherapy
What is the most common form of myasthenia gravis in dogs and how can it present?
- Generalised - most common
- Fulminant - acute onset and rapidly progressive
- Focal - megaoesophagus
Akitas, GSD, German shorthaired pointers, chihuahua
What are the common presentations of myasthenia gravis in the cat?
- Generalised
- Secondary to a thymoma
Abyssinian cats
How can you diagnose myasthenia gravis?
Anti-nicotinic acetyl choline receptor antibodies
Positive edrophonium test
How can you treat myasthenia gravis and what is the prognosis?
Anticholinesterases
- pyridostigmine PO
- neostigmine IM
Immunosuppression using corticosteroids at a later stage - worsens px if aspiration pneumonia develops
Thymectomy if due to a thymoma
Megaoesophagus management - postural feeding, PEG tube
Guarded px - may recover in 6m
Fulminant form difficult to treat
What are the most common causative agents in infectious myositis?
Neospora
Toxoplasma
What are the clinical signs of immune mediate polymyositis?
Variable onset Exercise intolerance and general weakness Pyrexia Very severe myalgia Muscle atrophy Stiffness and reluctance to move Non-ambulatory tetraparesis
How can you diagnose immune mediate polymyositis?
Inflammatory leukogram
Elevated AST and CK
Muscle biopsies
Rule out infectious cause
How can you treat immune mediated polymyositis?
Immunosuppression
Prednisolone etc
What is the clinical presentation of masticatory myositis?
CKCS
Swollen and painful masticatory muscles
Exophthalmos
Masticatory muscle atrophy
How should you diagnose masticatory myositis?
Anti 2M antibodies
Muscle biopsy
Raised CK
How should you treat masticatory myositis?
Prednisolone
How does infectious myositis due to neospora usually present?
Puppies Polyradiculoneuritis Polymyositis Ascending paralysis of the PLs Pelvic limb hyperextension
How can you diagnose infectious myositis and how should you treat it?
Dx: serology
Tx: Clindamycin, TMPS, pyrimethamine