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Dejerine-Sottas disease is an inherited neurological disorder that progressively affects mobility. Peripheral nerves become enlarged or thickened leading to muscle weakness.
Dejerine-Sottas Disease
Friedreich's Ataxia
Diseases of the Neuromuscular Junction: ...
CMT3 or Dejerine-Sottas disease is a severe demyelinating neuropathy that begins in infancy. Infants have severe muscle atrophy, weakness, and sensory problems.
Vitamins, BPB (CBER), Accommodation, Zinc sulfate, Dejerine-Sottas Disease, Dentistry for Disabled, Device, Heart-Assist, Disorders, Sexual Aversion, Dizocilpine, Dociton, Emulsions, Facial Paralyses, Idiopathic, Foreign Body Reaction, Ganglions, ...
Also known as Dejerine-Sottas disease, CMT3 is a severe form of CMT that develops during infancy and affects the myelin sheath.
CMT4. This is the most complicated form of CMT.
Hereditary Peripheral Neuropathy; Dejerine-Sottas Disease
356.8 -
Peripheral Neuropathy, Other Specified Idiopathic; Supranuclear Paralysis ...
Acute or chronic demyelinating polyneuropathy
Porphyria
Paraneoplatic syndromes
Genetic disorders ( Charcot-Marie-Tooth disease , Dejerine-Sottas disease, and Refsum’s disease)
Prolonged treatment in the intensive care unit ...
This type of CMT is less common and occurs after adolescence.
Type III-Also called Dejerine-Sottas disease, this is a more rare, severe, early onset form of CMT. It is sometimes considered to be a subtype of CMT Type I. Symptoms may include: ...
 See also: Symptom, Muscle weakness, Weakness, Atrophy, Injury
  
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