X-linked hypophosphatemia. Genetic and clinical correlates
Hanna, J.D.; Niimi, K.; Chan, J.C.
American Journal of Diseases of Children 145(8): 865-870
1991
ISSN/ISBN: 0002-922X PMID: 1858722 Document Number: 387906
X-linked hypophosphataemia is a hereditary form of rickets that results from an isolated renal tubular wasting of phosphate. The clinical features unique to this disorder, the recent advances in the understanding of vitamin D metabolism and molecular genetics in X-linked hypophosphataemia, and treatments for the disorder are reviewed.
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