Hypoparathyroidism in Beta-Thalassemia Children in Relation to Bone Mineral Density
Irene Mokhtar Kamel;
Abstract
Thalassemia is a hereditary disease caused by defective
globin synthesis resulting in abnormal and/or decreased globin
quantity. Although the multitransfusion and chelation therapy
increased the life expectancy of thalassemia major ™
patients, it indu
globin synthesis resulting in abnormal and/or decreased globin
quantity. Although the multitransfusion and chelation therapy
increased the life expectancy of thalassemia major ™
patients, it indu
Other data
| Title | Hypoparathyroidism in Beta-Thalassemia Children in Relation to Bone Mineral Density | Other Titles | نقص هرمون الباراثيرويد فى الأطفال مرضى أنيميا البحر المتوسط (ب) وعلاقته بكثافة العظام | Authors | Irene Mokhtar Kamel | Keywords | Hypoparathyroidism in Beta-Thalassemia Children in Relation to Bone Mineral Density | Issue Date | 2011 | Description | Thalassemia is a hereditary disease caused by defective globin synthesis resulting in abnormal and/or decreased globin quantity. Although the multitransfusion and chelation therapy increased the life expectancy of thalassemia major ™ patients, it indu |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 103622p3123.pdf | 409.32 kB | Adobe PDF | View/Open |
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