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Haab-Dimmer型角膜营养不良合并Fuchs综合征目前国内外尚无报道。我们曾见一家系,现报告如下。先证者Ⅲ 1,男,45岁。主诉双眼无明显诱因视力逐渐下降7年。患者自幼虹膜呈灰色,早年曾测视力为1.5(双)。1983年起双眼视力开始下降,看书约1小时即感眼张、眼花、头痛。体检未见异常。眼部检查:视力:右0.3.J6。右0.1.J6。一眼固视时,另一眼的角膜映光点偏向角膜中点的内侧约20°,双眼结膜无充血。双眼角膜实
Haab-Dimmer corneal dystrophy with Fuchs syndrome at home and abroad have not been reported. We have seen a family, the report is as follows. The proband Ⅲ 1, male, 45 years old. The main complaint of no obvious cause of binocular eyesight gradually decreased for 7 years. The patient’s iris was gray in his early years, with a measured early vision of 1.5 (double). Eyesight began to decline in 1983, about 1 hour reading that Zhang eyes, vertigo, headache. No abnormal physical examination. Eye examination: visual acuity: right 0.3.J6. Right 0.1.J6. A fixation, the other corneal reflection point to the midpoint of the cornea about 20 ° medial, conjunctival hyperemia. Eyes corneal real