Shams Fatemeh, Livingstone Iain, Oladiwura Dilys, Ramaesh Kanna
Department of Ophthalmology, Gartnavel General Hospital, Glasgow, Scotland.
Clin Ophthalmol. 2014 Oct 10;8:2077-84. doi: 10.2147/OPTH.S36626. eCollection 2014.
Cystinosis is a rare autosomal recessive disorder characterized by the accumulation of cystine within the cells of different organs. Infantile nephropathic cystinosis is the most common and severe phenotype. With the success of renal transplantation, these patients are now living longer and thus more long-term complications within different organs are becoming apparent. Ophthalmic manifestations range from corneal deposits of cystine crystals to pigmentary retinopathy. With increasing age, more severe ocular complications have been reported. Photophobia is a prominent symptom for patients. With prolonged survival and increasing age, this symptom, along with corneal erosions and blepharospasm, can become debilitating. This review revisits the basic pathogenesis of cystinosis, the ocular manifestations of the disease, and the treatment of corneal crystals.
胱氨酸病是一种罕见的常染色体隐性疾病,其特征是不同器官的细胞内胱氨酸蓄积。婴儿型肾病性胱氨酸病是最常见且最严重的表型。随着肾移植的成功,这些患者现在寿命更长,因此不同器官内的更多长期并发症正变得明显。眼部表现从胱氨酸晶体的角膜沉积到色素性视网膜病变不等。随着年龄增长,已报告有更严重的眼部并发症。畏光是患者的一个突出症状。随着生存期延长和年龄增长,该症状以及角膜糜烂和眼睑痉挛会变得使人衰弱。本综述重新审视了胱氨酸病的基本发病机制、该疾病的眼部表现以及角膜晶体的治疗。