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  Vol. 145 No. 8, August 1991 TABLE OF CONTENTS
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X-lined Hypophosphatemia

Genetic and Clinical Correlates

James D. Hanna, MD; Kazuhiko Niimi, MD; James C. M. Chan, MD

Am J Dis Child. 1991;145(8):865-870.


Abstract

• 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.

(AJDC. 1991;145:865-870)



Author Affiliations

From the Department of Pediatrics and Children's Medical Center, Virginia Commonwealth University's Medical College of Virginia, Richmond.


Footnotes

Accepted for publication January 24, 1991.

Reprint requests to Box 498, MCV Station, Richmond, VA 23298-0498 (Dr Chan).



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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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