医学
身材矮小
女孩
骨质疏松症
颅面
骨骼疾病
儿科
双膦酸盐
外科
牙科
内科学
精神科
心理学
发展心理学
作者
Assimina Galli‐Τsinopoulou,Ioannis Kyrgios,Styliani Giza,Eleni Z. Giannopoulou,Ioanna Maggana,Nikolaos Laliotis
出处
期刊:PubMed
日期:2012-09-01
卷期号:37 (3): 283-9
被引量:28
摘要
Hajdu-Cheney syndrome (HCS) is a rare disorder principally characterized by acro-osteolysis, distinctive craniofacial and skull changes, dental anomalies and short stature. A common finding in HCS patients is secondary osteoporosis that progresses over time and contributes to various skeletal problems, especially fractures. Although autosomal dominant inheritance has been documented in several families, sporadic (non-familial) cases have also been reported. Here, a case of a 9-year-old girl with familial HCS and multiple spinal fractures, who has been effectively treated with pamidronate, is presented. This is the first report of a beneficial effect of intravenous bisphosphonate administration on a child with HCS-related osteoporosis.
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