Idiopathic intracranial hypertension in cystinosis

被引:35
作者
Dogulu, CF
Tsilou, E
Rubin, B
FitzGibbon, EJ
Kaiser-Kupper, MI
Rennert, OM
Gahl, WA
机构
[1] NICHD, Lab Clin Genom, NIH, Bethesda, MD 20892 USA
[2] NEI, Ophthalm Clin Genet Sect, Ophthalm Genet & Visual Funct Branch, Acu Sect,Lab Sensorimotor Res,NIH, Bethesda, MD 20892 USA
[3] NHGRI, Sect Human Biochem Genet, Med Genet Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.jpeds.2004.06.080
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives To report a high frequency of idiopathic intracranial hypertension (IIH) in patients with cystinosis and to speculate on the relationship between these two disorders. Study design Retrospective case series and review of the literature regarding risk factors for the development of IIH in cystinosis. Results Eight patients with cystinosis had documented papilledema, normal neuroimaging of the brain, cerebrospinal fluid (CSF) opening pressure greater than 200 mm of H2O, and normal CSF composition. No common medication, condition, or disease except cystinosis was found in these persons. Six of the patients had received prednisone, growth hormone, cyclosporine, oral contraceptives, vitamin D, or levothyroxine at the time of onset of IIH. Five patients had previous renal transplants. Conclusion No single risk factor for the development of IIH linked IIH to cystinosis in our patients. However, thrombosis susceptibility as a result of renal disease or impaired CSF reabsorption in the arachnoid villi as a result of cystine deposition might lead to the development of IIH in cystinosis.
引用
收藏
页码:673 / 678
页数:6
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