Costil J, Debard A, Guilhaume A, Charpentier C, Pousset J L, Brissaud H E
Sem Hop. 1980;56(1-2):22-7.
Two cases of propionicacidemia are reported. The first patient was a child aged 16 months with psychomotor retardation, severe disturbances of wakefulness, and vomiting; the second case concerned a new-born baby with metabolic acidosis and neurological disorders. In both cases the diagnosis of propionicacidemia was made after the discovery of ketonuria, and raised blood ammonia and glucose levels. Appropriate dietary measures led to great improvement in the first case, and nearly normal psychomotor development in the second case at 7 months of age. Problems related to biotin sensitivity, leucine intolerance, and raised blood ammonia levels are discussed.
报告了两例丙酸血症病例。首例患者为一名16个月大的儿童,有精神运动发育迟缓、严重的觉醒障碍和呕吐症状;第二例是一名患有代谢性酸中毒和神经障碍的新生儿。两例患者均在发现酮尿症以及血氨和血糖水平升高后确诊为丙酸血症。采取适当的饮食措施后,首例患者病情大为改善,第二例患者在7个月大时精神运动发育近乎正常。文中还讨论了与生物素敏感性、亮氨酸不耐受和血氨水平升高相关的问题。