Physiotherapy Neurological Rehabilitation
Genetic
Myotonia conjenita
- Thowsen Disease (from birth)
- Becker Myotonia (from 4-6 yo)
Muscular dystrophy
- Duchenne muscle dystrophy
- Myotonic dystrophy
- Becker muscular dystrophy
- Limb girdle muscular dystrophy
- Facioscapulohumeral muscle dystrophy
Peripheral
Charcot Marie tooth
Dejerine-Scottas syndrome
Motor
Spinal Muscular Atrophy
Motor neuron disease
- amyotrophic lateral sclerosis (both UMN and LMN)
- progressive bulbar palsy (IX glossopharingeal, X vagus, XII hypoglossal)
- progressive muscular atrophy (only LMN)
- primary lateral sclerosis (only UMN)
Huntington disease
Progressive supranuclear palsy
Tay-Sachs disease (late onset)
Kennedys disease
Infection
Encephalitis
Meningitis
Transverse Myelitis
Post polio syndrome
Autoimmune
gullian barre syndrome
chronic inflammatory demyelinating polyneuropathy
multiple sclerosis
myasthenia gravis
Lupus
Tumors
brain tumor
neurofibromatosis
Tauma
TBI
Spinal Cord
Vascular
Stroke
transient ischaemic attack
Developmental (Brain)
Arteriovenous malformation
cerebral palsy
hydrocephalus
dystonia
Parkinson disease
dementia
conversion disorder
Symptoms
Myopathy (musculoskeletal, neuromuscular, rheumatic (myositis), infection, metabolic (hypokalemia), trauma, endocrine (thyroid, adrenal), toxic)
Apraxia
ataxia
dyskinesia
Vestibular
acoustic neuroma
being paroxysmal positional vertigo – BPPV
labirintitis
vertigo
vestibular migrane
vestibular neuritis
meniere’s disease