See Also: Westphal's disease(medicine)
Strumpell-Westphal disease(medicine)
heterospecific(medicine)
heterospecific graft(medicine)
heterospecific antibody(medicine)
Herbal medicine (botanical medicine, herbology, phytomedicine)(health)
Erb-Westphal sign(medicine)
Westphal's phenomenon(medicine)
Westphal's pseudosclerosis(medicine)
Westphal's sign(medicine)

heterospecific antibody (medicine) and Westphal's disease (medicine)


heterospecific antibody (medicine)


heterospecific antibody
<immunology> Artificially produced antibody in which the two antigen binding sites are for different antigens.


Westphal's disease (medicine)


Westphal's disease -->
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.