Article
A clinical and molecular genetic study of hypophosphatemic rickets in children.
Pediatric research - 1 Aug 2005
Cho Hee Y, Lee Bum H, Kang Ju H, Ha Il S, Cheong Hae I, Choi Yong
Abstract excerpt
X-linked hypophosphatemic rickets (XLH), autosomal dominant hypophosphatemic rickets, hereditary hypophosphatemic rickets with hypercalciuria, and tumor-induced osteomalacia share clinical and biochemical features, and are collectively referred to as hypophosphatemic rickets (HR). Recently, the molecular bases of HR were elucidated. A review of medical records and mutational analyses of the PHEX and FGF23 genes...
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