Jonas A J, Conley S B, Marshall R, Johnson R A, Marks M, Rosenberg H
Department of Pediatrics, University of Texas Medical School, Houston 77030.
Am J Med. 1987 Nov;83(5):966-70. doi: 10.1016/0002-9343(87)90661-9.
Nephropathic cystinosis is associated with end-stage renal failure, retinal damage, and hypothyroidism. Patients may now survive past the first decade of life with the use of dialysis and renal transplantation. Examination of a 24-year-old woman with this disorder revealed ovarian failure, mildly abnormal results on a glucose tolerance test, intermittent confusion, short-term memory loss, and cerebral atrophy on computerized axial tomography. Autopsy examination at age 25 years revealed cystine storage in multiple tissues including the atrophic ovaries, pancreatic islet cells, the aorta, and the brain. Dysfunction of multiple organ systems may develop in patients with cystinosis who survive into adulthood. This emphasizes the need for a systemic therapy for cystinosis.
肾病性胱氨酸病与终末期肾衰竭、视网膜损害和甲状腺功能减退有关。现在,通过透析和肾移植,患者可以存活到十岁以后。对一名患有这种疾病的24岁女性进行检查发现,她存在卵巢功能衰竭、葡萄糖耐量试验结果轻度异常、间歇性意识模糊、短期记忆丧失以及计算机断层扫描显示脑萎缩。25岁时的尸检显示,胱氨酸储存在多个组织中,包括萎缩的卵巢、胰岛细胞、主动脉和大脑。存活至成年的胱氨酸病患者可能会出现多器官系统功能障碍。这凸显了对胱氨酸病进行系统性治疗的必要性。