X linked hypophosphataemia: treatment, height gain, and nephrocalcinosis.

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X linked hypophosphataemia: treatment, height gain, and nephrocalcinosis.

The clinical data of 18 patients with X linked hypophosphataemia were analysed retrospectively. The height data were expressed as SD scores. There was no difference in the final height of patients treated with vitamin D (or 1,25-dihydroxyvitamin D) and phosphate for at least two years (n = 12) and that of 16 hypophosphataemic family members who had never been treated. The mean final SD score (-...

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X-linked hypophosphataemia in South Africa.

OBJECTIVES To investigate the pattern of clinical presentation in a series of South African subjects with X-linked hypophosphataemia (XLH) with particular reference to ethnic differences in presentation and inheritance, and to determine the perceptions and psychosocial problems associated with the disease. DESIGN AND SETTING The clinical details of 50 subjects were collected from their record...

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Thiazide diuretics arrest the progression of nephrocalcinosis in children with X-linked hypophosphatemia.

OBJECTIVE X-linked hypophosphatemia (XLH) is characterized clinically by rickets, hypophosphatemia, and hyperphosphaturia. Conventional treatment of XLH with oral phosphate and vitamin D is associated with increased urinary calcium excretion and nephrocalcinosis. Thiazide diuretics decrease urinary calcium excretion. The objective of this study was to determine the effect of thiazide diuretics ...

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Treatment of hypophosphataemic rickets in children remains a challenge.

INTRODUCTION Hypophosphataemic rickets (HR) is a rare hereditary disease characterised by hypophosphataemia, defects in bone mineralisation and rickets. MATERIAL AND METHODS We searched the hospital files at H.C. Andersen Children's Hospital, Odense University Hospital, Denmark, for children with the International Classification of Diseases 10 codes E83.3B (vitamin D resistant rickets) and E8...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1990

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.65.10.1125