期刊
CHILDREN-BASEL
卷 10, 期 6, 页码 -出版社
MDPI
DOI: 10.3390/children10061072
关键词
molybdenum cofactor deficiency; inborn error metabolism; MRI; metabolic
类别
Molybdenum cofactor deficiency (MoCD) is a rare and severe autosomal recessive inborn error of metabolism caused by gene mutations, resulting in neurotoxicity and early neurodegeneration. MRI is the imaging of choice for diagnosis, showing characteristic radiological findings such as diffuse cerebral edema, infarction, and multicystic encephalomalacia. Our case report presents a novel contrast-enhanced MRI pattern characterized by diffuse and linear leptomeningeal enhancement, which was performed to exclude an infectious disease. Early identification of MoCD is crucial for prompt and effective management of the complications.
Molybdenum cofactor deficiency (MoCD) is a rare and severe autosomal recessive in-born error of metabolism caused by the mutation in MOCS1, MOCS2, MOCS3 or GEPH genes, with an incidence ranging between 1 in 100,000 and 200,000 live births. The clinical presentation with seizures, lethargy and neurologic deficits reflects the neurotoxicity mediated via sulphite accumulation, and it occurs within the first hours or days after birth, often leading to severe neurodegeneration and the patient's death within days or months. The Imaging of Choice is a brain-specific MRI technique, which is usually performed without contrast and shows typical radiological findings in the early phase, such as diffuse cerebral oedema and infarction affecting the cortex and the basal ganglia and the white matter, as well as in the late phase, such as multicystic encephalomalacia. Our case report represents a novelty in the field, since the patient underwent a contrast-enhanced MRI to exclude a concomitant infectious disease. In the frame of the clinical presentation and laboratory data, we describe the MoCD Imaging findings for MRI morphological and advanced sequences, presenting a new contrast-enhanced MRI pattern characterized by the diffuse and linear leptomeningeal enhancement of brain, cord and spinal roots. The early identification of molybdenum cofactor deficiency is crucial because it may lead to the best multidisciplinary therapy for the patient, which is focused on the prompt and optimal management of the complications.
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