000			02150nam a22003137a 4500
001			CUHAS/MD/4000918/T/12
003			CUHAS/MD/4000918/T/12
005			20240305193823.0
008			210804b |||||||| |||| 00| 0 eng d
028			_bWurzburg Road 35, BMC Premises, Post Code: 33102:
028			_bP. O. Box 1464, Mwanza – Tanzania:
028			_b Phone: +255 28 298 3384:
028			_bFax: +255 28 298 3386:
028			_bEmail: vc@bugando.ac.tz :
028			_b www.bugando.ac.tz
035			_aCUHAS/MD/4000918/T/12
040			_bEnglish _cDDC
041			_aEnglish
041			_aKiswahili
100			_a Salum, Halima _dCUHAS/MD/4000918/T/12 _920442
245			_aManagement of Sickle Cell Disease in Paediatric Population Hospitalized at Temeke Regional Hospital.
260			_aMwanza, Tanzania: _bCatholic University of Health and Allied Sciences [CUHAS – Bugando] : _c©2017
300			_a vii; 28 Pages
300			_aIncludes References
520			_aAbstract: Background: The term sickle cell disease (SCD) describes a group of inherited red blood cell disorders. People with SCD have abnormal hemoglobin called hemoglobin S or sickle hemoglobin in their RBCs. Many children with SCD die before age of 5 years due to low level of hemoglobin and infections. Also lack of newborn screening programs in sub Saharan countries lead to late diagnosis hence some of them die without knowing they have SCD. Objectives: To increase knowledge on management of SCD and its complications, also to determine common presentation of SCD. Methodology: Prospective observation study involving children from 4 to 59 months admitted at pediatric ward at Temeke regional hospital from 1st to 30th September who were be followed from admission to know on how a comprehensive management to SCD is well provided and how children respond to treatment. Implication of the study: To improve my knowledge on diagnosis and comprehensive management of SCD as is a major health problem in our society.
600			_xPediatrics and Child Health
700			_a Ambrose, Emmanuela. E _920275
942			_2ddc _cCR
999			_c20581 _d20581