Bartsocas C S, Zeis P M, Elia M, Papadatos C J
Ann Genet. 1982;25(1):61-2.
a 12 1/2-year-old boy with the rare autosomal recessive syndrome of osteoporosis with pseudoglioma is reported. Pertinent laboratory findings included osteoporotic lesions of the skeleton and calcification of the left lens. He was hypotonic and presented atrophic globes with opacities of the lenses. His psychomotor development was normal. Parental consanguinity is not excluded.
报告了一名12岁半患有罕见的骨质疏松伴假性胶质瘤常染色体隐性综合征的男孩。相关实验室检查结果包括骨骼的骨质疏松性病变和左眼晶状体钙化。他肌张力减退,眼球萎缩,晶状体混浊。其精神运动发育正常。不排除父母近亲结婚。