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Author

Lama Alwahiby

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Review Open access Oct 2026

Congenital/Inherited CD59 Deficiency: A Systematic Review

Background: Inherited CD59 deficiency is a rare autosomal recessive complement-mediated disorder caused by biallelic loss-of-function variants in the CD59 gene. It typically presents in infancy with Coombs-negative hemolytic anemia, relapsing demyelinating polyneuropathy, and recurrent ischemic strokes. Diagnosis is of...

Lama Alwahiby, Lanah Alsuhim, Manal Alzahrani et al. · 0 citations

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