Neuhäuser G, Kaveggia E G, Opitz J M
Clin Genet. 1976 Mar;9(3):324-32. doi: 10.1111/j.1399-0004.1976.tb01581.x.
We report a sibship of three sisters and two brothers who showed osteoporosis of variable severity; the propositus has incapacitating deformities following numerous fractures. Four of the sibs, including three with frequent fractures, were blind from infancy ("pseudogliomatous blindness"). In addition, two were mentally retarded. The osteoporosis-pseudoglioma syndrome is inherited as an autosomal recessive trait; similar reports from the literature support this assumption.
我们报告了一个有三姐妹和两兄弟的家庭,他们表现出不同程度的骨质疏松症;先证者因多次骨折而出现致残性畸形。其中四个兄弟姐妹,包括三个经常骨折的,自幼失明(“假性胶质瘤性失明”)。此外,还有两人智力发育迟缓。骨质疏松-假性胶质瘤综合征以常染色体隐性性状遗传;文献中的类似报告支持这一假设。