Melobroxidase deficiency:
It is relatively common and inherited as an autosomal recessive. Melobroxidase is a component of neutrophil-loving neutrophil granules. The production of oxalide and other toxic media is important for the cytotoxic function, the topical meloproxidase gene on the chromosome 17.
Clinical manifestations:
- Disturbance of killing neutrophils of bacteria and bacteria abroad.
- The percentage of bacterial infections does not increase.
- Deep Candida infections.
- The supplemental deficiency
- Supplementary deficiency C1 Astrase.
Clinical manifestations:
- Bacterial infections.
- Increased susceptibility to infections, especially for double-gram negatives such as nazeria.
- autoimmune diseases.
- The lack of early compounds through the classic activation of the supplement leads to different clinical manifestations depending on the pattern of incomplete complement.
It is relatively common and inherited as an autosomal recessive. Melobroxidase is a component of neutrophil-loving neutrophil granules. The production of oxalide and other toxic media is important for the cytotoxic function, the topical meloproxidase gene on the chromosome 17.
Clinical manifestations:
- Disturbance of killing neutrophils of bacteria and bacteria abroad.
- The percentage of bacterial infections does not increase.
- Deep Candida infections.
- The supplemental deficiency
- Supplementary deficiency C1 Astrase.
Clinical manifestations:
- Bacterial infections.
- Increased susceptibility to infections, especially for double-gram negatives such as nazeria.
- autoimmune diseases.
- The lack of early compounds through the classic activation of the supplement leads to different clinical manifestations depending on the pattern of incomplete complement.
