Brown E S, Waisman H A, Geison R L, Gerritsen T
Helv Paediatr Acta. 1977 Nov;32(4-5):401-11.
Histidinemia was found in 3 of 4 siblings in one family, while a fatal encephalopathy with mental retardation was present in two of them and in the fourth child who did not have histidinemia. Biochemical studies of the histidinemic subjects showed elevated histidine levels in urine, CSF, and brain, while in a few urine samples histidine related imidazole compounds were found. Plasma levels of other amino acids were positively correlated with plasma histidine levels. Obesity and heart abnormalities appeared to be associated with the encephalopathy, which is probably of a new type. The histidinemia appears to be unrelated to the mental retardation or the encephalopathy in this family.
在一个家庭的4个兄弟姐妹中,有3人被发现患有组氨酸血症,其中2人以及没有组氨酸血症的第4个孩子患有伴有智力发育迟缓的致命性脑病。对患有组氨酸血症的受试者进行的生化研究表明,其尿液、脑脊液和大脑中的组氨酸水平升高,同时在一些尿液样本中发现了与组氨酸相关的咪唑化合物。其他氨基酸的血浆水平与血浆组氨酸水平呈正相关。肥胖和心脏异常似乎与这种可能是新型的脑病有关。在这个家庭中,组氨酸血症似乎与智力发育迟缓或脑病无关。