Osteoporosis in Thalassemia Major-Reflection in Indian Scenario
Beta-thalassemia represents a group of recessively inherited hemoglobin disorders first described by Cooley and Lee and characterized by reduced synthesis of ß-globin chain. Homozygous state results in severe anemia, which needs regular blood transfusion. Life expectancy of thalassemia patients extended dramatically, by combination of transfusion and chelation therapy in-turn it give rise to various complications severe hepatosplenomegaly, bone marrow expansion, growth retardation, congestive heart failure bone deformity or even death. Osteoporosis is common even in well-treated thalassemic patients. There is only handful of data reflecting t…
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Produktdetails
Weitere Autoren: Kumar, Ashok
- ISBN: 978-613-8-82970-6
- EAN: 9786138829706
- Produktnummer: 31648362
- Verlag: Blues Kids Of Amer
- Sprache: Englisch
- Erscheinungsjahr: 2019
- Seitenangabe: 160 S.
- Masse: H22.0 cm x B15.0 cm x D1.0 cm 256 g
- Gewicht: 256
Über den Autor
Dr. Kritanjali Singh, working as Research officer and HOD at Central Research Station in Subharti Medical College, Meerut. Persued PhD from SGPGIMS. Qualified ICMR-Self SRF, grant from UP-Gov. and ICMR, New Delhi.
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