Marrakchi S, Lasram L, Bouguila H, Barbirou I, Ouertani A, Ayed S
Service d'Ophtalmologie, Institut Hedi Rais d'Ophtalmologie de Tunis, Tunisie.
J Fr Ophtalmol. 1994;17(4):238-41.
The authors reported ten cases of familial nephropathy (two cystinosis, three Senior and Loken syndrome, one Alport's syndrome and four Oxalosis) associated to ocular manifestations. Aetiologic diagnosis was known from ocular symptoms in five cases (all cases of cystinosis and Senior and Loken syndrome). The authors undertook this study to analyse the value of ocular manifestations in determining the right aetiologic diagnosis in familial nephropathies. The results of this study showed that ocular manifestations are helpful for aetiologic diagnosis in the first diseases. Indeed, corneal injury is synonym of cystinosis and retinitis pigmentosa is usually associated with Senior and Loken syndrome. In Alport's syndrome, ocular manifestations: antcrior lenticonus cataractous and perimacular white points only have orientation value in the diagnosis of this disease. Oxalosis ocular manifestations which consist of retinal oxalate deposits appear late and are concomitant to familial renal insufficiency. They cannot help in the diagnostic search.
作者报告了10例伴有眼部表现的家族性肾病(2例胱氨酸病、3例Senior和Loken综合征、1例Alport综合征和4例草酸尿症)。5例(所有胱氨酸病和Senior和Loken综合征病例)的病因诊断可根据眼部症状得出。作者开展这项研究以分析眼部表现在确定家族性肾病正确病因诊断方面的价值。这项研究结果表明,眼部表现在最初的疾病中有助于病因诊断。确实,角膜损伤是胱氨酸病的同义词,而色素性视网膜炎通常与Senior和Loken综合征相关。在Alport综合征中,眼部表现:前圆锥形晶状体混浊和黄斑周围白点仅在该疾病诊断中具有指导价值。由视网膜草酸盐沉积构成的草酸尿症眼部表现出现较晚,且与家族性肾功能不全同时出现。它们无助于诊断。