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Physiotherapy Neurological Rehabilitation

Genetic

Muscles

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

 

Nerves

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)

 

Brain

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