Polland W, Nordström S
Acta Ophthalmol (Copenh). 1979 Aug;57(4):653-64. doi: 10.1111/j.1755-3768.1979.tb00514.x.
Two families from northern Sweden with a total of 8 patients with typical symptoms of congenital achromatopsia with amblyopia were studied. In one of the families 4 affected children (3 brothers and 1 sister) also showed pallor of the optic discs and marked astigmatism. The transmission of the disease was consistent with an autosomal recessive inheritance in both families. The study confirmed that complete and incomplete achromatopsia might be different expressions of the same gene. Six out or 13 near relatives of the achromatic patients showed minor colour vision defects, suggesting a tendency towards heterozygotic manifestation of the gene.
对瑞典北部的两个家族进行了研究,这两个家族共有8名患有先天性全色盲并伴有弱视典型症状的患者。在其中一个家族中,4名患病儿童(3名兄弟和1名姐妹)还表现出视盘苍白和明显的散光。两个家族中该疾病的遗传方式均符合常染色体隐性遗传。该研究证实,完全性和不完全性全色盲可能是同一基因的不同表现形式。13名全色盲患者的近亲中有6名表现出轻微的色觉缺陷,提示该基因存在杂合子表现的倾向。