Rickets: It's not just vitamin D deficiency

Current Opinion in Endocrinology and Diabetes

Volumn 8, Issue 1, 2001, Pages 23-28

  Hochberg, Z ^a  

^a RAMBAM MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

25 HYDROXYVITAMIN D; 25 HYDROXYVITAMIN D 24 HYDROXYLASE; CALCIDIOL 1 MONOOXYGENASE; CALCITRIOL; CALCIUM; COLECALCIFEROL HYDROXYLASE; KIDNEY ENZYME; OXYGENASE; PHOSPHATONIN; PHOSPHORUS; PROTEINASE; RETINOL; TUMOR PROTEIN; UNCLASSIFIED DRUG; VITAMIN D; VITAMIN D RECEPTOR;

ALGORITHM; CALCIUM DEFICIENCY; CHILD; DIAGNOSTIC PROCEDURE; DISEASE CLASSIFICATION; ENZYME ACTIVITY; GENE MUTATION; HUMAN; HYDROXYLATION; HYPOPHOSPHATEMIA; MALNUTRITION; OSTEOMALACIA; REVIEW; RICKETS; SKIN COLOR; TUMOR; VITAMIN D DEFICIENCY; VITAMIN D METABOLISM; VITAMIN METABOLISM;

EID: 0035141957     PISSN: 10683097     EISSN: None     Source Type: Journal    
DOI: 10.1097/00060793-200102000-00005     Document Type: Review

References (41)

1. Vitamin D deficiency rickets: Socio-demographic and clinical risk factors in children seen at referral hospital in Addis Ababa
2. An investigation into a possible relationship between vitamin D, parathyroid hormone, calcium and magnesium in a normally pigmented and an albino rural black population in the Northern Province of South Africa
3. A high prevalence of metabolic bone disease in exclusively breastfet very low birthweight infants in Dar-es-Salaam, Tanzania
4. Vitamin D deficiency and nutritional rickets in children
5. A comparison of calcium, vitamin D or both for nutritional rickets in Nigerian children
6. Nutritional rickets without vitamin D deficiency in Bangladesh
7. Calcium-enriched foods and bone mass growth in prepubertal girls: A randomized, double-blind, placebo-controlled trial
8. Bone abnormalities in gastrointestinal and hepatic disease
9. Pre and post-treatment serum levels of cytokines IL-1β, IL-6 and IL-1 receptor antagonist in Celiac disease: Are they related to the associated osteopenia?
10. Bone mineral content in infants and children with chronic cholestatic liver disease
11. Renal bone disease: Radiological investigation
12. 25-Hydroxyvitamin D3 1α-Hydroxilase and vitamin D synthesis
13. The role of vitamin D receptor in regulating vitamin D metabolism: A study in calcitriol-resistant rickets
14. Vitamin A antagonizes the action of vitamin D in rats
15. Characterization of human sterol 27-hydroxylase
16. Partial deletion of the gene encoding sterol 27-hydroxylase in a subject with cerebrotendineous xanthomatosis
17. Molecular cloning od cDNA and genomic DNA for human 25-hydroxyvitamin D 1α-hydroxylase
18. The promoter of the human 25-hydroxyvitamin D 1 alpha-hydroxylase gene confers positive and negative responsiveness to PTH, calcitonin and 1 alpha, 25(OH)2D3
19. Genetic mutation in the human 25-hydroxyvitamin D31α-hydroxylase gene cause vitamin D-dependent rickets type I
20. Genetic causes of rickets
21. Enzymatic properties of mouse 25-hydroxyvitamin D31α-hydroxylase expressed in Escherichia Coli
22. No enzyme activity of 25-hydroxyvitamin D31α-hydroxylase gene product in pseudovitamin D deficiency rickets, including that with mild clinical manifestation
23. Mouse vitamin D-24-hydroxilase. Molecular cloning, tissue distribution, and transcriptional regulation by 1-α,25-dihydroxvitamin D3
24. Vitamin-D resistant rickets with alopecia: Cultured skin fibroblasts exhibit defective cytoplasmic receptors and unresponsiveness to 1,25(OH)2D3
25. Calcitriol resistant rickets due to vitamin D receptor defects
26. In vivo function of VDR in gene expression-VDR knock-out mice
27. Calcium therapy in calcitriol resistant rickets
28. Rescue of the skeletal phenotype of vitamin D receptor-ablated mice in the setting of normal mineral ion homeostasis: Formal histomorphometric and biomechanical analyses
29. New insight into the pathogenesis of inherited phosphate wasting disorders
30. A gene (PEX) with homologies to endopeptidase is mutated in patients with X-linked hypophosphatemic rickets
31. PHEX gene and hypophosphatemia
32. Mutational analysis of PHEX gene in X-linked hypophosphatemia
33. Coordinated maturational regulation of PHEX and renal phosphate transport inhibitory activity: Evidence for the pathophysiological role of PHEX in X-linked hypophosphatemia
34. Intrinsic mineralization defect in hypnouse osteoblasts
35. A PHEX gene mutation is responsible for adult-onset vitamin D resistant hypophosphatemic osteomalacia: Evidence that the disorder is not distinct entity from X-linked hypophosphatemic rickets
36. Familial hypophosphatemic rickets showing autosomal dominant inheritance
37. Aotosomal dominant hypophosphatemic rickets/osteomalacia: Clinical characterization of a novel phosphate wasting syndrome
38. Inhibition of renal phosphate transport by a tumor product in a patient with oncogenic osteomalacia
39. "Idiopathic" hypercalciuria and hereditary hypophosphatemic rickets. Two phenotypical expressions of a common genetic defect
40. Rickets