Malan C, Neethling A C, Shanley B C, Gompertz D, Bartlett K, Schraader E B
S Afr Med J. 1977 Jun 25;51(26):980-3.
Two siblings who were repeatedly admitted to hospital with acute episodes of vomiting, dehydration and coma were found to be suffering from isovaleric acidaemia. This condition is a rare inherited abnormality of leucine metabolism, which is frequently fatal in the early weeks of life and leads to mental retardation in a high proportion of those who survive early attacts. However, both our patients were of normal intelligence. The clinical presentation, biochemical defect, diagnosis and suggested therapies are reviewed.
两名兄弟姐妹因反复出现呕吐、脱水和昏迷的急性发作而多次入院,结果发现他们患有异戊酸血症。这种病症是一种罕见的亮氨酸代谢遗传性异常,在生命的最初几周通常是致命的,并且在很大比例的早期发病存活者中会导致智力发育迟缓。然而,我们的两名患者智力均正常。本文对其临床表现、生化缺陷、诊断及建议的治疗方法进行了综述。