De Bandt M, Meyer O, Fuster J M, Kahn M F
Rheumatology Unit, Hôpital Bichat, Paris, France.
J Rheumatol. 1995 Jul;22(7):1395-8.
We describe a 52-year-old man who presented with diffuse idiopathic skeletal hyperostosis, ossification of the posterior longitudinal ligament, and abnormal levels of retinol and retinol binding protein (RBP). The molar retinol/retinol binding protein ratio was high, suggesting congenital functional RBP deficiency. His two sons, aged 23 and 27 years, shared the same biological abnormality without clinical symptoms. To our knowledge, this is the first case report of such a familial association.
我们描述了一名52岁男性,他患有弥漫性特发性骨肥厚、后纵韧带骨化以及视黄醇和视黄醇结合蛋白(RBP)水平异常。视黄醇/视黄醇结合蛋白的摩尔比很高,提示先天性功能性RBP缺乏。他的两个儿子,分别为23岁和27岁,也有相同的生物学异常,但无临床症状。据我们所知,这是首例关于这种家族关联的病例报告。