| type II h. |
that resulting from antibody-antigen interactions on cell surfaces; see type II hypersensitivity reaction, under hypersensitivity reaction, at reaction. Called also antibody-mediated h.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| type II i. |
i.-γ.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type II t. |
DNA topoisomerase (ATP-hydrolyzing).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type III |
amylo-1,6-glucosidase deficiency: an autosomal recessive disorder caused by a defect in the debranching enzyme in muscle, liver, or both; defects in the liver enzyme are characterized by hepatomegaly and hypoglycemia, while defects in the muscle enzyme are characterized by progressive muscle wasting and weakness. Heart and skeletal muscle are also frequently affected. Called also debrancher deficiency.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| type III c.’s |
a group of immune complexes involving polyclonal immunoglobulins, usually globulin-antiglobulin complexes, found in infectious diseases and autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus, and Sjögren's syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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