3 ফলাফল
Hereditary hypophosphatemia (XLH) is a rare, inherited disease. Loss-of-function mutation in PHEX results in excess fibroblast growth factor 23 (FGF23) production and manifests as rickets in children and osteomalacia in adults. FGF23 is a hormone that reduces renal phosphate reabsorption, decreases
Patients All patients starting active end stage renal disease (ESRD) treatment at the participating centres and their satellite centres.
No. Patients: 1000.
1. Patients who have received their recent predialysis care at another centre can be included if the previous centre's notes are available,
AIMS AND OBJECTIVES:
- To study GH-IGF1 axis in children with CML having short stature following Imatinib therapy.
- To administer growth hormone therapy to children with CML on Imatinib in remission having GH deficiency.
STUDY DESIGN: It is an interventional, non-randomized study. STUDY GROUP: one