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Імунодефіцит, зумовлений дефіцитом класичного компонента шляху комплементу

ORPHA:169147· ICD-10 D84.1· Immunodeficiency due to a classical component pathway complement deficiency

Визначення(English summary)

A rare primary immunodeficiency due to a deficiency in either complement components C1q, C1r, C1s, C2 or C4 characterized by increased susceptibility to bacterial infections, particularly with encapsulated bacteria, and increased risk for autoimmune disease. Most commonly, these include systemic lupus erythematosus (SLE), SLE-like disease, Henoch-Schonlein purpura, polymyositis and arthralgia. Disease severity is variable and dependent on the complement affected.

Успадкування
Autosomal recessive