Results 181 to 190 of about 4,392 (235)
Diagnosis, treatment, and management of rickets: a position statement from the Bone and Mineral Metabolism Group of the Italian Society of Pediatric Endocrinology and Diabetology [PDF]
De Sanctis, Luisa, Tessaris, Daniele
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A Rare Case of Pediatric X-Linked Hypophosphatemic Rickets: Challenges and Insights from Pakistan
Raamish Aamir Khan +4 more
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LOCALIZATION OF THE GENE CAUSING X-LINKED HYPOPHOSPHATEMIC RICKETS
Thakker, R +13 more
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X-linked hypophosphatemic rickets without ?rickets?
Skeletal Radiology, 1991Wrist and knee radiographs from children with X-linked hypophosphatemic rickets were analyzed and compared with those from normal children and children with established rickets to assess whether radiographically apparent rickets is a consistent abnormality in X-linked hypophosphatemia. The absence or presence of rickets was correctly identified in 94.8%
M J, Econs +8 more
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Therapeutics of X-linked hypophosphatemic rickets
Pediatric Nephrology, 1993X-linked hypophosphatemia, the most common form of familial rickets, is conventionally treated with 1,25-dihydroxyvitamin D3 (5-50 ng/kg per day) plus phosphate supplementation (70-100 mg/kg per day). However, nephrocalcinosis is noted in many children treated with this therapy.
K, Latta, S, Hisano, J C, Chan
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Growth in X-linked hypophosphatemic rickets
European Journal of Pediatrics, 2006Growth failure appears frequently in children with X-linked hypophosphatemic rickets (XLHR) due to hypophosphatemia, disease severity, body disproportion, and primary bone abnormality. Recombinant human growth hormone (rhGH) increases phosphate tubular reabsorption and phosphate level in blood and, thus, constitutes an attractive but controversial ...
Gema, Ariceta, Craig B, Langman
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Hearing impairment in familial X-linked hypophosphatemic rickets
European Journal of Pediatrics, 2004Hearing impairment in patients with X-linked dominant hypophosphatemic rickets (XLH) is likely part of the natural history of the disease, developing during adulthood. Therefore, whereas close follow up and hearing monitoring is recommended in adults, serial audiograms in children with XLH are not justified. Furthermore, in a child with XLH and hearing
Gadi, Fishman +4 more
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