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Complement 2 deficiency

human disease

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General referenceInterpretive dossier study · Crown Archives visual atlas
Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJul 17, 2025
Entity authorityQ5156399
Source-derived summary

Complement 2 deficiency is a type of complement deficiency caused by any one of several different alterations in the structure of complement component 2.

It has been associated with an increase in infections.

It can present similarly to systemic lupus erythematosus (SLE).

Signs and symptoms

C2D is linked to bacterial infections, especially encapsulated bacterial infections, as well as a risk of Systemic Lupus Erythematosus (SLE) or SLE-like disease.

Complement deficiency has historically been associated with early, severe bacterial infections among children. Infection susceptibility is frequently observed.

C2D is linked to abnormalities in serum immunoglobulin levels, such as lower IgG2 and IgG4 levels, which could contribute to raised infection susceptibility. More than half of 40 C2D patients in a study had Streptococcus pneumoniae-related invasive infection, primarily meningitis or sepsis. Haemophilus influenza type b and Neisseria meningitis are two other infections commonly seen in C2D patients.

Complications

In roughly 10% of patients, a C2 deficiency is linked to an illness that resembles SLE. Clinical manifestations of this SLE-like illness include fever, rash, arthritis, and glomerulonephritis.

Editorial summary

“Complement 2 deficiency” enters the record as human disease. Crown Archives preserves that source wording while asking what Complement, deficiency and human can confirm, complicate or overturn.

Editorial reviewA dependable orientation record for establishing vocabulary, names and a first evidence trail. The current 173-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. Its strongest next move is a source search built around Complement, deficiency and human.
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“Complement 2 deficiency” is worth following because a concise public description often conceals a longer documentary argument. Here, Complement, deficiency and human provides the most credible route into that argument.

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Vocabulary and entity names are the principal evidence signals here, because they determine the precision of every later search. The source revision retrieved here is dated Jul 17, 2025. The linked authority identifier is Q5156399.

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Source & attribution

This entry incorporates text from Complement 2 deficiency” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.