1 results match your criteria: "Tokyo Metropolitan Kiyose Children's Hospital Endocrinology and Metabolism Division[Affiliation]"
[Hypophosphatemic rickets/osteomalacia. - Mainly on patients with PHEX mutations -].
Clin Calcium
October 2007
Tokyo Metropolitan Kiyose Children's Hospital Endocrinology and Metabolism Division, Research Laboratory.
Most patients with inherited hypophosphatemic Rickets/Osteomalacia have mutations in the PHEX gene. In this brief review, we focus on the treatment for patients with this mutation. First, molecular basis of inherited hypophosphatemic Rickets/Osteomalacia, followed by pathophysiology of PHEX and its related disorders is described.
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