Article

Two Mild Phenotype Molybdenum Cofactor Deficiency Patients with Novel MOCS2 Mutation and Immunological Treatment after COVID-19 Infection

2025-09-17

Abstract excerpt

<title>Abstract</title> <p> Background Molybdenum cofactor deficiency type B (MoCD-B) is a rare autosomal recessive metabolic disorder caused by mutations in the MOCS2 gene. Patients with mild phenotypes may experience infection-related neurological deterioration followed by partial spontaneous recovery. This study presents the first reported cases of acute encephalopathy triggered by SARS-CoV-2 infection in pat...

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Literature Corpus work: 773ff6b3-080f-5bff-8a81-1e296bed71a0
DOI: 10.21203/rs.3.rs-7278913/v1

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