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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease thalassemia
Comorbidity C0029456|osteoporosis
Sentences 9
PubMedID- 25216685 Iron overload causes osteoporosis in thalassemia major patients through interaction with transient receptor potential vanilloid type 1 (trpv1) channels.
PubMedID- 25849944 The reported frequency of osteoporosis, in thalassemia mayor patients, despite adequate transfusion and iron chelation therapy, varies from 13.6% to 50% with an additional 45% affected by osteopenia [67].
PubMedID- 20976089 The pathogenesis of osteoporosis in thalassaemia major (tm) is complicated and differs from the pathogenesis of bone deformities characteristically found in nontransfused patients who develop bone distortion mainly due to ineffective haemopoiesis and progressive marrow expansion [3].
PubMedID- 22778734 Subjects in low pubertal staging and short stature(<3% percentile) have significantly lower bone mass densities p < 0.001. conclusion.he prevalence of osteoporosis is high in patients with thalassemia major, possibly related to delayed puberty.
PubMedID- 24575552 osteoporosis in thalassemia major: an update and the i-cet 2013 recommendations for surveillance and treatment.
PubMedID- 22581647 We conclude that circulating sclerostin is elevated in thalassemia patients with osteoporosis and correlated with their bmd, but it was not reduced post zoledronic acid administration.
PubMedID- 22966867 Prospective study of histomorphometry, biochemical bone markers and bone densitometric response to pamidronate in beta-thalassaemia presenting with osteopenia-osteoporosis syndrome.
PubMedID- 20694183 In a study by otrock et al,60 18 thalassemia patients with osteoporosis were given zol 4 mg iv every 3 months over a period of 12 months.
PubMedID- 25002928 Haticehamarat, et al studied frequency of osteoporosis in thalassemia major patients in turkey and showed that among25 patients with thalassemia major (14 men, 11 women) 16 patients had osteoporosis, where as 9 patients had osteopenia (18).

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