CELIAC DISEASE AND VITAMIN D DEPENDENT RICKETS TYPE I. CASE REPORT

被引:0
|
作者
Lesanu, G. [1 ,2 ]
Becheanu, C. [1 ]
Olteanu, B. S. [3 ]
Oraseanu, D. [1 ]
机构
[1] Grigore Alexandrescu Emergency Pediat Hosp, Dept Pediat, Bucharest 011743, Romania
[2] Carol Davila Univ Med & Pharm, Dept Pediat, Bucharest, Romania
[3] Grigore Alexandrescu Emergency Pediat Hosp, Dept Radiol, Bucharest 011743, Romania
关键词
celiac disease; vitamin D dependent rickets type I; child; SKELETAL-MUSCLE TISSUE; D; 1-ALPHA-HYDROXYLASE; D DEFICIENCY; DIAGNOSIS; GENE;
D O I
10.4183/aeb.2010.381
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Case report. A 5 year 2 months old boy was admitted in our hospital for failure to thrive, muscle weakness, bowing of legs, walking difficulties. At the age of 14 months he had been investigated for failure to thrive. Clinical, biochemical and radiologic signs were suggestive for rickets. Positive celiac serology and histology of the small bowel were consistent with the diagnosis of celiac disease (CD). Treatment included parenteral vitamin D and gluten free diet. The parents did not accept the diet, but the child received a daily vitamin D supplementation of 1000 IU. At. the age of 4 years celiac serology was positive and the second duodenal biopsy was normal. Physical examination, biochemical data, and rachitic changes on x-ray were compatible with the diagnosis of rickets. Clinically severe rickets, hypocalcemia, elevated level of PTH. demonstrating secondary hyperparathyroidism, and low level of calcitriol determined the diagnosis of vitamin D-dependent rickets type (VDDR-I). Although being on a normal diet, tissue antitransglutaminase antibodies were negative, but HLA genotyping showed DQ2 positive. In conclusion, the patient presented the diagnosis of VDDR-I associated with latent celiac disease. The VDDR-I was masked by CD, rickets being attributed to malabsorption.
引用
收藏
页码:381 / 386
页数:6
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