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磷酸化酶激酶缺乏症患者的生化特征及四糖苷排泄增加

Biochemical characteristics and increased tetraglucoside excretion in patients with phosphorylase kinase deficiency.

作者信息

Morava E, Wortmann S B, van Essen H Zweers, Liebrand van Sambeek R, Wevers R, van Diggelen O P

机构信息

Department of Pediatrics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

J Inherit Metab Dis. 2005;28(5):703-6. doi: 10.1007/s10545-005-0095-9.

Abstract

Patients with glycogen storage disease type IXa present with infantile hepatomegaly and a specific growth pattern, and variable biochemical alterations in blood. We studied the clinical and biochemical characteristics including the urinary oligosaccharide excretion of seven unrelated children. The urinary tetraglucoside excretion was increased in four children, three of whom had persistently high cholesterol and triglyceride concentrations. We propose screening for urine tetraglucoside excretion and the measurement of serum cholesterol in patients with growth delay and/or hepatomegaly to assess a possible glycogenosis.

摘要

IXa型糖原贮积病患者表现为婴儿期肝肿大和特定的生长模式,血液中存在可变的生化改变。我们研究了7名无亲缘关系儿童的临床和生化特征,包括尿寡糖排泄情况。4名儿童的尿四糖苷排泄增加,其中3名儿童的胆固醇和甘油三酯浓度持续偏高。我们建议对生长发育迟缓及/或肝肿大的患者进行尿四糖苷排泄筛查和血清胆固醇测定,以评估是否可能患有糖原贮积病。

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