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Cranial MRI of an infant with glutathione synthetase deficiency (1)

There was a wide range of long T1 signals in the bilateral frontotemporal parietal lobes. The lesions on both sides are roughly symmetrical. (Source: Wu X, Jiao J, Xia Y, et al. Case report: a Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation. Front Pediatr 2023;11:1212405. Creative Commons Attribution [CC BY] license.)

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