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Kritanjali Singh

Osteoporosis in Thalassemia Major-Reflection in Indian Scenario

Buch

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… Mehr

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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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