for uncompetitive inhibition
for competitive inhibition
for non competitive inhibition
Methionine synthase
Clinical significance
Mutations in the MTR gene have been identified as the underlying cause of methylcobalamin deficiency complementation group G, or methylcobalamin deficiency cblG-type.[1] The consequence of reduced methionine synthase activity ismegaloblastic anemia.
AUTOIMMUNE HEMOLYTIC ANEMIA
Drug induced AIHA is also a rare cause of the disease. It can be caused by a number of drugs including α-methyldopa and penicillin. This is a type II immune response in which the drug binds to macromolecules on the surface of the RBC and acts as an antigen. Antibodies are produced against the RBC and lead to complement activation. Complement fragments such as C3a, C4a and C5a activate granular leukocytes (e.g. neutrophils); while other components of the system (C6, C7, C8, C9) can either form the membrane attack complex (MAC) or can bind the antibody stimulating phagocytosis by macrophages (C3b). This is one type of "penicillin allergy"
甲醇(Methyl Alcohol).
Most of the symptoms of Kartagener syndrome result from the inability of the respiratory cilia to function correctly, such as:
- Chronic sinus infection
- Frequent lung infections, such as pneumonia and bronchitis
- Bronchiectasis - lung damage from frequent infections
- Frequent ear infections
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