Takahashi T, Kodama S, Nishio H, Takumi T, Matsuo T, Hase Y, Sawada Y
J Inherit Metab Dis. 1985;8(3):105-8. doi: 10.1007/BF01819290.
A case of transient hyperphenylalaninaemia with a maturational delay of dihydropteridine synthesis is described. With the Guthrie test, the patient showed a blood phenylalanine level of 38 mg dl-1, which had fallen to a normal value without a phenylalanine restricted diet by 3 months of age. The neopterin level and the neopterin to biopterin ratio in the patient's urine were very high at 19 days of age. The blood phenylalanine level did not decrease when tetrahydrobiopterin (2.5 mg kg-1) was administered at 19 days of age, while administration of tetrahydrobiopterin (7.5 mg kg-1) at 20 days of age had decreased the blood phenylalanine level to 50% of the preloading level after 24 h. The oral phenylalanine loading test showed the pattern of classic phenylketonuria (PKU) at 15 days of age, but it showed the normal pattern at 1 year 8 months of age.
本文描述了一例伴有二氢蝶啶合成成熟延迟的短暂性高苯丙氨酸血症病例。通过格思里试验,该患者的血苯丙氨酸水平为38mg/dl,在3月龄时未采用限制苯丙氨酸饮食的情况下已降至正常水平。患者在19日龄时尿中新蝶呤水平及新蝶呤与生物蝶呤的比值非常高。在19日龄时给予四氢生物蝶呤(2.5mg/kg),血苯丙氨酸水平未降低,而在20日龄时给予四氢生物蝶呤(7.5mg/kg),24小时后血苯丙氨酸水平降至负荷前水平的50%。口服苯丙氨酸负荷试验在15日龄时显示为典型苯丙酮尿症(PKU)模式,但在1岁8月龄时显示为正常模式。