Severe hypercalcemia associated with Williams syndrome successfully treated with pamidronate infusion therapy

被引:9
作者
Sangun, Ozlem [1 ]
Dundar, Bumin N. [1 ]
Erdogan, Elvan [2 ]
机构
[1] Suleyman Demirel Univ, Fac Med, Dept Pediat Endocrinol, TR-32260 Isparta, Turkey
[2] Suleyman Demirel Univ, Fac Med, Dept Pediat, TR-32260 Isparta, Turkey
关键词
hypercalcemia; pamidronate infusion therapy; Williams syndrome;
D O I
10.1515/JPEM.2011.113
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Infantile hypercalcemia becomes manifest in 15% of patients with Williams syndrome (WS) and generally is not clinically severe. However, some patients with WS can have severe hypercalcemia and do not respond well to traditional therapies. Recently, pamidronate has been used in the treatment of childhood hypercalcemia associated with many disorders, but there is little experience with the treatment of hypercalcemia with bisphosphonates in patients with WS. We present a 17-month-old female patient, who had been diagnosed as WS by genetic analysis, admitted to our clinic for the investigation of severe hypercalcemia (4.02 mmol/L). Because the patient did not respond very well to fluid administration, furosemide infusion, and dietary calcium restriction, pamidronate infusion was performed and calcium levels returned to normal within 2 days. This case report is presented to point out that pamidronate therapy seems to be a safe and efficient way of treating life-threatening hypercalcemia in WS.
引用
收藏
页码:69 / 70
页数:2
相关论文
共 7 条
[1]   Severe infantile hypercalcemia associated with Williams syndrome successfully treated with intravenously administered pamidronate [J].
Cagle, AP ;
Waguespack, SG ;
Buckingham, BA ;
Shankar, RR ;
DiMeglio, LA .
PEDIATRICS, 2004, 114 (04) :1091-1095
[2]  
CHESNEY RW, 1989, CLIN DISORDERS BONE, P395
[3]  
Cunniff C, 2001, PEDIATRICS, V107, P1192
[4]  
LOWERY MC, 1995, AM J HUM GENET, V57, P49
[5]   Long-term control of hypercalcaemia in an infant with Williams-Beuren syndrome after a single infusion of biphosphonate (Pamidronate) [J].
Oliveri, B ;
Mastaglia, SR ;
Mautalen, C ;
Gravano, JC ;
Argerich, LP .
ACTA PAEDIATRICA, 2004, 93 (07) :1002-1003
[6]  
Wu YQ, 1998, AM J MED GENET, V78, P82, DOI 10.1002/(SICI)1096-8628(19980616)78:1<82::AID-AJMG17>3.0.CO
[7]  
2-K