Yalvaç I S, Altintas A K, Gökdere A, Duman S
Eye Department of Ankara Hospital, Turkey.
Acta Ophthalmol Scand. 1998 Apr;76(2):243-4. doi: 10.1034/j.1600-0420.1998.760225.x.
We report a case of bilateral retinitis pigmentosa simplex (RP) with a combination of unilateral Fuchs' heterochromic uveitis (FHU). Both of these entities are quite rare syndromes and coexistence of these entities in one patient is rarer than can be expected. Even though this rare coexistence came together in one patient, we found no hereditary factors to presume that both traits segregate independently.
我们报告了一例双侧单纯性视网膜色素变性（RP）合并单侧富克斯异色性葡萄膜炎（FHU）的病例。这两种病症均为相当罕见的综合征，而在同一患者中同时存在这两种病症的情况比预期更为罕见。尽管这种罕见的共存情况出现在了一名患者身上，但我们并未发现遗传因素可推测这两种特征是独立分离的。
