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Minerva Endocrinol ; 37(3): 283-9, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22766895

ABSTRACT

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.


Subject(s)
Abnormalities, Multiple , Bone Density Conservation Agents/administration & dosage , Bone Density/drug effects , Diphosphonates/administration & dosage , Hajdu-Cheney Syndrome/drug therapy , Osteoporosis/drug therapy , Acro-Osteolysis/drug therapy , Child , Drug Administration Schedule , Female , Follow-Up Studies , Hajdu-Cheney Syndrome/genetics , Hajdu-Cheney Syndrome/pathology , Humans , Infusion Pumps , Osteoporosis/genetics , Osteoporosis/pathology , Osteoporotic Fractures/etiology , Pamidronate , Pedigree , Spinal Fractures/drug therapy , Spinal Fractures/genetics , Spinal Fractures/prevention & control , Time Factors , Treatment Outcome
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