Experience of treating familial hypophosphatemic rickets with activated vitamin D(1.ALPHA.-OH-D3).

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چکیده

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Familial Hypophosphatemic Rickets: Pathophysiology and Medical Management

Chronic hypophosphatemia is one major cause of rickets and osteomalacia in growing children (see Preface of this volume). There are acquired and congenital forms. In most instances, the acquired forms can be controlled by acting on the underlying cause (insufficient phosphate intake, increased renal loss secondary to a mesenchymal tumor, or an altered renal tubular function). The inherited synd...

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We report the development of severe tertiary hyperparathyroidism in three girls treated for familial hypophosphatemic rickets and characterize parathyroid function in vivo and in vitro. All patients had been previously treated with relatively large doses of inorganic phosphorus (125 mm/day) and ergocalciferol or calcitriol for several years and had radiographic evidence of long-standing hyperpa...

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Familial Hypophosphatemic Rickets - A Case Report and Review of Literature

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Metabolism of vitamin D3-3H in vitamin D-resistant rickets and familial hypophosphatemia.

The fate of an intravenous dose of tritiated vitamin D(3) was studied in seven normal subjects, four children with vitamin D-resistant rickets, and four adults with a familial history of vitamin D-resistant rickets and persistent hypophosphatemia. An abnormal metabolism of vitamin D in vitamin D-resistant rickets was defined and characterized by a decrease in the plasma fractional turnover rate...

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ژورنال

عنوان ژورنال: Orthopedics & Traumatology

سال: 1985

ISSN: 1349-4333,0037-1033

DOI: 10.5035/nishiseisai.34.713