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  Vol. 145 No. 8, August 1991 TABLE OF CONTENTS
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X-linked hypophosphatemia. Genetic and clinical correlates

J. D. Hanna, K. Niimi and J. C. Chan
Department of Pediatrics, Virginia Commonwealth University's Medical College of Virginia, Richmond.

X-linked hypophosphatemia is a hereditary form of rickets that results from an isolated renal tubular wasting of phosphate. The clinical features unique to this disorder, and the recent advances in our understanding of vitamin D metabolism and molecular genetics in X-linked hypophosphatemia are reviewed. Finally, a succinct critique of the controversial treatment modalities round up this review.

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Normal Growth and Muscle Dysfunction in X-Linked Hypophosphatemic Rickets Associated with a Novel Mutation in the PHEX Gene
Makras et al.
J. Clin. Endocrinol. Metab. 2008;93:1386-1389.
ABSTRACT | FULL TEXT  





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