See Also: lenticular progressive degeneration(medicine)
progressive bulbar paralysis(medicine)
Erb spinal paralysis(medicine)
spinal paralysis(medicine)
spastic spinal paralysis(medicine)
progressive spinal amyotrophy(medicine)
progressive spinal muscular atrophy(medicine)
infantile progressive spinal muscular atrophy(medicine)
progressive infantile spinal muscular atrophy(medicine)
Herbal medicine (botanical medicine, herbology, phytomedicine)(health)

lenticular progressive degeneration (medicine) and spinal paralysis (medicine)


lenticular progressive degeneration (medicine)


lenticular progressive degeneration -->
Wilson's disease
<gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure.

Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common.

Inheritance: autosomal recessive.


spinal paralysis (medicine)


spinal paralysis


Loss of motor power due to a lesion of the spinal cord.

Synonym: myeloparalysis, myeloplegia, rachioplegia.