Brismar J, Aqeel A, Gascon G, Ozand P
Department of Radiology, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
AJNR Am J Neuroradiol. 1990 Jan-Feb;11(1):135-8.
A defect in biopterin synthesis not only prevents the transformation of phenylalanine to tyrosine (as in classical phenylketonuria, PKU) but also blocks the biosynthesis of the neurotransmitters dopamine, norepinephrine, and serotonin, causing severe neurologic disturbances. The brain CT and MR findings in this rare disorder have not been described. In the present series, eight patients with PKU were all examined with CT, three were also examined with MR imaging. In spite of severe clinical findings, CT was normal or almost normal in three patients; in three other children, moderate loss of brain volume was found. White matter disease was found in three patients (moderate in two and severe in one) and was also found in an additional patient with classical PKU. PKU should therefore be added to the list of possible causes for white matter disease. Furthermore, biopterin-dependent PKU should be considered when the CT examination in a child with severe neurologic manifestation only shows discrete pathology.
生物蝶呤合成缺陷不仅会阻止苯丙氨酸向酪氨酸的转化(如经典型苯丙酮尿症,PKU),还会阻碍神经递质多巴胺、去甲肾上腺素和血清素的生物合成,从而导致严重的神经功能障碍。这种罕见疾病的脑部CT和MR表现尚未见报道。在本系列研究中,8例PKU患者均接受了CT检查,其中3例还接受了MR成像检查。尽管临床表现严重,但3例患者的CT结果正常或几乎正常;另外3名儿童发现有中度脑容量减少。3例患者发现有白质病变(2例中度,1例重度),1例经典型PKU患者也发现有白质病变。因此,PKU应被列入白质病变可能的病因清单。此外,当仅有严重神经症状表现的儿童CT检查仅显示轻微病变时,应考虑生物蝶呤依赖性PKU。