Article

Late-onset Renal involvement presenting with TMA and tubular injury in cobalamin C disease: a report of three cases and review of the literature

2023-10-10

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Mutation of methylmalonic aciduria type C and homocystinuria (<italic>MMACHC</italic>) gene causes inherited cobalamin C disease (cblC), an inborn error of cobalamin metabolism, which presents with methylmalonic aciduria (MMA) and homocystinuriain clinical. Renal complications may also be present in patients with this inborn deficiency. The most common histologi...

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Literature Corpus work: 5b6bbf47-bdec-5c29-b749-a76e2f71b805
DOI: 10.21203/rs.3.rs-3394380/v1

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