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Erschienen in: Current Osteoporosis Reports 4/2011

01.12.2011 | Pediatrics and Skeletal Development (Craig Langman and Maria Luisa Bianchi, Section Editors)

Rickets

verfasst von: M. Zulf Mughal

Erschienen in: Current Osteoporosis Reports | Ausgabe 4/2011

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Abstract

Rickets is disorder of a growing child arising from disorders that result in impaired apoptosis of hypertrophic cells and mineralization of the growth plate. Rickets due to nutritional causes remains an important global problem. The factors responsible for resurgence of rickets among dark-skinned infants living in developed countries include the following: residence in northern or southern latitudes, voluntary avoidance of exposure to solar ultraviolet B radiation, maternal vitamin D deficiency during pregnancy, and prolonged breastfeeding without provision of vitamin D supplements. Fibroblast growth factor 23 (FGF23), secreted by osteocytes, is an important regulator of serum phosphate and 1,25(OH)2D3 levels. Hypophosphatemic rickets resulting from increased synthesis or under-catabolism of FGF23 is reviewed.
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Zurück zum Zitat Phulwani P, Bergwitz C, Jaureguiberry G, Rasoulpour M, Estrada E. Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutation. Am J Med Genet A. 2011;155A(3):626–33.PubMed Phulwani P, Bergwitz C, Jaureguiberry G, Rasoulpour M, Estrada E. Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutation. Am J Med Genet A. 2011;155A(3):626–33.PubMed
Metadaten
Titel
Rickets
verfasst von
M. Zulf Mughal
Publikationsdatum
01.12.2011
Verlag
Current Science Inc.
Erschienen in
Current Osteoporosis Reports / Ausgabe 4/2011
Print ISSN: 1544-1873
Elektronische ISSN: 1544-2241
DOI
https://doi.org/10.1007/s11914-011-0081-0

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