Revision as of 20:34, 26 April 2023 edit Brendamarteenez (talk \| contribs) 32 edits →Complement Component 2 Deficiency ← Previous edit		Revision as of 20:36, 26 April 2023 edit undo Brendamarteenez (talk \| contribs) 32 edits →Conclusion Next edit →
Line 30: == Conclusion == Photosensitive patients with C2 type I deficiency have poor prognosis. C2 type I deficiency is caused by a 28-base pair gene deletion, resulting in premature termination codon and lack of C2 protein.Patients with LE associated with complement C4 or C2 deficiencies have a better prognosis than those without inherited deficiencies. Overall, Complement component 2 deficiency increases risk of autoimmune disorders and may be managed by receiving the adequate care. == References ==

Complement component 2: Difference between revisions