Meny R G, Gutberlet R L, Ozand P, Morris C, Kim C H
Am J Dis Child. 1978 Mar;132(3):261-2. doi: 10.1001/archpedi.1978.02120280045009.
We discuss an infant with hepatitis and hypermethioninemia. An inborn error of metabolism, such as methionine adenosyltransferase deficiency or hereditary tyrosinemia, was originally thought to be the basis for these abnormalities. The infant's subsequent clinical course, however, was incompatible with such a diagnosis; the hypermethioninemia was instead due to the trilogy of prematurity, hepatitis, and a high-protein, high-methionine diet.
我们讨论了一名患有肝炎和高甲硫氨酸血症的婴儿。最初认为,诸如甲硫氨酸腺苷转移酶缺乏症或遗传性酪氨酸血症等先天性代谢缺陷是这些异常情况的基础。然而,该婴儿随后的临床病程与这种诊断不符;高甲硫氨酸血症反而归因于早产、肝炎以及高蛋白、高甲硫氨酸饮食这三个因素。