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Four Cases of X-Linked Hypophosphatemic Rickets, Clinical Description and Genetic Testing
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作者 David Vila-Pérez Sílvia Marín-del-Barrio +3 位作者 Jordi Vila-Cots Jose Antonio Camacho-Díaz Marcos Morey lourdes loidi 《Open Journal of Genetics》 2014年第1期40-45,共6页
One of the major causes of congenital hypophosphatemic rickets is the X-linked hypophosphatemic rickets (XHR), due to a defect on PHEX gene. The XHR increases the renal elimination of phosphate, that condition leads a... One of the major causes of congenital hypophosphatemic rickets is the X-linked hypophosphatemic rickets (XHR), due to a defect on PHEX gene. The XHR increases the renal elimination of phosphate, that condition leads a defective mineralization of bones and also affects the growth in children. Clinical diagnosis should be suspected in children with signs of rickets and hypophosphatemia with normal calcium levels. We describe clinical characteristics and genetic results of four patients diagnosed and treated in our Nephrology Section. All patients have a “de novo” XHR as none familiars are affected. Early diagnosis should be suspected before the bone deformities have been submitted and the growth would have been impaired. 展开更多
关键词 RICKETS X-LINKED Hypophosphatemic RICKETS XHR PHEX Gene
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