Moreira-Filho C A, Neustein I
J Med Genet. 1979 Apr;16(2):125-8. doi: 10.1136/jmg.16.2.125.
The present report describes a Brazilian Negro sibship with six males affected by a presumptive new variant of Norrie's disease, an X-linked congenital oculo-acoustical-cerebral degeneration. In addition to the typical stigmata of the disease, all the patients were microcephalic and two of them had cryptorchidism. Possible non-genetic aetiology was investigated with negative results. Xg blood group studies were informative and the lod scores are given, together with those for two previously reported families with Norrie's disease.
本报告描述了一个巴西黑人同胞家族,其中有6名男性患有一种推测为诺里病新变种的疾病,这是一种X连锁先天性眼-耳-脑变性疾病。除了该疾病的典型体征外,所有患者均为小头畸形,其中2人患有隐睾症。对可能的非遗传病因进行了调查,结果为阴性。Xg血型研究提供了信息,并给出了连锁分析计分,以及两个先前报道的患有诺里病的家族的连锁分析计分。