Acute hemolytic anemia as an initial presentation of wilson's disease /
Amerah Mohamed Ahmed Elshahawy
Acute hemolytic anemia as an initial presentation of wilson's disease / أنيميا إنحلال الدم الحادة كعرض أولى لمرض ويلسون Amerah Mohamed Ahmed Elshahawy ; Supervised Mona Elsaid Elraziky , Mona Mohamed Hamdy , Amal Abdelhamid Ali - Cairo : Amerah Mohamed Ahmed Elshahawy , 2012 - 123 P. : facsimiles ; 25cm
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics
Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point in time during the natural course of illness. The aim of current study was to screen for WD among children presenting HA
Hemolytic anemia Initial presentation Wilson's disease
Acute hemolytic anemia as an initial presentation of wilson's disease / أنيميا إنحلال الدم الحادة كعرض أولى لمرض ويلسون Amerah Mohamed Ahmed Elshahawy ; Supervised Mona Elsaid Elraziky , Mona Mohamed Hamdy , Amal Abdelhamid Ali - Cairo : Amerah Mohamed Ahmed Elshahawy , 2012 - 123 P. : facsimiles ; 25cm
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics
Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point in time during the natural course of illness. The aim of current study was to screen for WD among children presenting HA
Hemolytic anemia Initial presentation Wilson's disease