HYPOPHOSPHATASIA IN AN ADULT - A CASE-REPORT

被引:0
作者
NANGAKU, M
SATO, N
SUGANO, K
TAKAKU, F
机构
关键词
ALKALINE PHOSPHATASE; BONE MINERALIZATION; GENETIC DISEASE; OSTEOCALCIN; METABOLIC BONE DISEASE;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:47 / 52
页数:6
相关论文
empty
未找到相关数据