Nangaku M, Sato N, Sugano K, Takaku F
Third Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Jpn J Med. 1991 Jan-Feb;30(1):47-52. doi: 10.2169/internalmedicine1962.30.47.
In this rare case of adult hypophosphatasia, no radiological abnormalities of the skeletal system could be detected even by dual energy X-ray absorptiometry. Severe dental caries was the sole clinical manifestation, indicating this case as an "odontohypophosphatasia". The levels of serum osteocalcin were low, which may be a useful biochemical marker to diagnose hypophosphatasia. Southern blot analyses of the genomic DNA revealed no gross abnormalities. Thus, hypophosphatasia in this patient was presumed to be caused by point mutations or small deletions. In a review of previous reports, an increased incidence among women was found.
在这例罕见的成人低磷酸酯酶症病例中,即便采用双能X线吸收法也未检测到骨骼系统的放射学异常。严重龋齿是唯一的临床表现,表明该病例属于“牙型低磷酸酯酶症”。血清骨钙素水平较低,这可能是诊断低磷酸酯酶症的一项有用的生化指标。对基因组DNA进行的Southern印迹分析未发现明显异常。因此,推测该患者的低磷酸酯酶症是由点突变或小片段缺失引起的。在回顾既往报告时,发现女性中的发病率有所增加。