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经典瓜氨酸血症患者 30 年随访结果。

30-year follow-up of a patient with classic citrullinemia.

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Mol Genet Metab. 2012 Jun;106(2):248-50. doi: 10.1016/j.ymgme.2012.03.011. Epub 2012 Mar 23.

Abstract

Citrullinemia is a urea cycle defect requiring long-term care with nutritional and pharmacological management. Despite treatment, morbidity and mortality of this disease remain high, and long-term complications include mild to profound mental retardation, seizures, and growth deficiency. We report a 31-year old woman with classic, neonatal-onset citrullinemia who developed progressive hypertrophic cardiomyopathy and cataracts, neither of which has been recognized previously as a complication of the disease or a consequence of long-term drug treatment.

摘要

瓜氨酸血症是一种尿素循环缺陷,需要长期的营养和药物管理。尽管进行了治疗,这种疾病的发病率和死亡率仍然很高,长期并发症包括轻度至重度智力迟钝、癫痫发作和生长发育不良。我们报告了一例 31 岁的经典型新生儿期瓜氨酸血症患者,她患有进行性肥厚型心肌病和白内障,但以前都没有认识到这是该疾病的并发症或长期药物治疗的后果。

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