Introduction: Hereditary spherocytosis is a red cell membrane disorder that causes hemolytic anemia. Due to defective cell membrane, red cells are spherical shaped and result in their early lysis. Osmotic fragility of spherocytic red cell is increased. Case report: A 22 year old female presented with chief complain of abdominal pain. Initially she was diagnosed as cholelithiasis. Under laboratory evaluation she was found to be anemic with reticulocytosis. In peripheral blood smear, spherocytes were moderately distributed. Antihuman globulin test was negative but osmotic fragility was high. Hence, she was confirmed as case of hereditary spherocytosis. Conclusion: Hereditary spherocytosis is a rare red cell disorder and its diagnosis ca...
Hereditary spherocytosis (HS) is an inherited abnormality of the red blood cell, caused by defects i...
Inherited forms of anaemia were only generally recognized at the turn of this century and Osler's te...
Abstract— Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity o...
Hereditary Spherocytosis (HS) is relatively common haemolytic anemia in which basic abnormality is ...
Hereditary Sperocytosis (HS) is a genetic disorder of RBC membrane proteins; resulting RBCs are sphe...
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in o...
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical...
peer reviewedA 12-year old female, suffering from recurring episodes of icterus and abdominal pain, ...
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical...
Hereditary spherocytosis (HS), a familial defect involving red blood cell (RBC) membrane proteins, i...
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical...
Hereditary spherocytosis is a clinically heterogeneous, genetically determined red blood cell membra...
This case report describes a 35-year-old lady who presented with generalized weakness and lethargy o...
Background: Hereditary spherocytosis is a very heterogeneous form of hemolytic anemia. The aim of th...
Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the...
Hereditary spherocytosis (HS) is an inherited abnormality of the red blood cell, caused by defects i...
Inherited forms of anaemia were only generally recognized at the turn of this century and Osler's te...
Abstract— Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity o...
Hereditary Spherocytosis (HS) is relatively common haemolytic anemia in which basic abnormality is ...
Hereditary Sperocytosis (HS) is a genetic disorder of RBC membrane proteins; resulting RBCs are sphe...
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in o...
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical...
peer reviewedA 12-year old female, suffering from recurring episodes of icterus and abdominal pain, ...
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical...
Hereditary spherocytosis (HS), a familial defect involving red blood cell (RBC) membrane proteins, i...
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical...
Hereditary spherocytosis is a clinically heterogeneous, genetically determined red blood cell membra...
This case report describes a 35-year-old lady who presented with generalized weakness and lethargy o...
Background: Hereditary spherocytosis is a very heterogeneous form of hemolytic anemia. The aim of th...
Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the...
Hereditary spherocytosis (HS) is an inherited abnormality of the red blood cell, caused by defects i...
Inherited forms of anaemia were only generally recognized at the turn of this century and Osler's te...
Abstract— Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity o...