IgA deficiency may be inherited as either an autosomal dominant (requiring only one parent to pass down the defective gene) or recessive (requiring defective genes from both parents) trait. It is found in approximately 1 in 700 individuals of European origin. It is less common in people of other ethnicities. Affected people often have chronic diarrhea caused by intestinal infections, and frequent respiratory infections. Many develop autoimmune diseases like rheumatoid arthritis and lupus erythematosus.
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