Fernandez-Sasso D, Acosta J E, Malbran E
Br J Ophthalmol. 1979 May;63(5):336-8. doi: 10.1136/bjo.63.5.336.
A new type of pre-Descemet's corneal dystrophy is described. The opacities are punctiform, polychromatic, of uniform size, and evenly distributed over the whole cornea. The diagnosis is made only by slit lamp because there is no visual impairment. The disease is hereditary and follows the autosomal mode of inheritance with a high percentage of penetrance, expressivity, and specificity in 4 successive generations, in which 8 affected members were observed among a total of 46.
描述了一种新型的Descemet膜前角膜营养不良。混浊为点状、多色性、大小均匀,且均匀分布于整个角膜。由于没有视力损害,仅通过裂隙灯进行诊断。该疾病具有遗传性,遵循常染色体遗传模式,在连续4代中具有高比例的外显率、表现度和特异性,在总共46名成员中有8名受影响成员。