Digenic Functional B12 and Folate Defect Mimicking Myelodysplasia

双基因功能性维生素B12和叶酸缺陷模拟骨髓增生异常综合征

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Abstract

A digenic defect involving CUBN and MTHFR produced functional B12/folate deficiency in a patient with pancytopenia and neurological signs, mimicking myelodysplasia. Genetic and metabolic screening revealed elevated methylmalonic acid/homocysteine, with rapid remission post-parenteral B12. This case highlights the need for metabolic/genetic workup in atypical cytopenias.

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