12-22-2009, 02:49 PM
A 15 month old girl is brought to the Doc. because of a 6 month history of progressive weakness and fatigue. Examination shows tachycardia, scleral icterus, pallor, hepatosplenomegaly. Her Hb conc. is 5.6 g/dl (N=11.5-14.5) and serum indirect Bili 3 mg/dl//
A peripheral blood smear shows severe hypochromia, nucleated Erys, microcytosis ..DNA analysis shows an A--->G point mutation within the TATA box of the B globulin ..
What is the lab in this patient:
Hb F increased
HbA2/Hb A Ratio Increased
Reti Increased
Anyone can please explain the lab findings
A peripheral blood smear shows severe hypochromia, nucleated Erys, microcytosis ..DNA analysis shows an A--->G point mutation within the TATA box of the B globulin ..
What is the lab in this patient:
Hb F increased
HbA2/Hb A Ratio Increased
Reti Increased
Anyone can please explain the lab findings