Paroxysmal Nocturnal Hemoglobinuria (PNH) is? a. hereditary b. congenital c. acquired d. autoimmune only
c
Paroxysmal Nocturnal Hemoglobinuria (PNH) is due to? a. ankyrin defect b. spectrin defect c. band 3 defect d. GPI anchor deficiency (protein)
d
Hereditary Spherocytosis (HS) defects in? a. ankyrin b. spectrin c. band 3 d. protein 4.2
a b c d
Hereditary Spherocytosis (HS) forms? a. elliptocytes b. stomatocytes c. target cells d. spherocytes
d
Hereditary Elliptocytosis (HE) defects in? a. spectrin b. protein 4.1 c. actin d. adducin
a b c d
Hereditary Elliptocytosis (HE) forms? a. elliptocytes b. spherocytes c. acanthocytes d. target cells
a
Rh null Syndrome is due to? a. GPI anchor deficiency b. glycophorin (A B) defects c. cholesterol defects d. absence of all Rh antigens
d
Rh null Syndrome leads to? a. aplastic anemia b. hemolytic anemia c. megaloblastic anemia d. polycythemia vera
b
Rh null Syndrome forms? a. stomatocytes b. target cells c. elliptocytes d. spherocytes
a b
Rh null Syndrome forms stomatocytes and target cells due to? a. decreased RBC production b. increased destruction of RBCs c. decreased hemoglobin synthesis d. increased iron
b
Glycophorin (A B) defects cause? a. severe hemolytic anemia b. mostly mild RBC shape changes c. acanthocyte formation d. spherocyte formation
b
Glycophorin (A B) defects cause altered malarial susceptibility with? a. increased susceptibility to P. falciparum b. resistance to P. falciparum c. resistance to P. vivax d. no change
b
Cholesterol defects lead to? a. spherocyte formation b. elliptocyte formation c. stomatocyte formation d. acanthocyte formation
d
Cholesterol defects causing acanthocytes involve? a. high levels only b. low levels only c. high or low levels d. normal levels
c
Cholesterol defects cause acanthocyte formation because cholesterol is part of the? a. RBC nucleus b. RBC membrane c. hemoglobin d. plasma proteins
b