A 9-year-old boy is brought to the physician by his mother for a 3-day history of increasingly yellowish discoloration of his eyes. He has no past medical history. He has not had any recent notable illnesses. He takes no medications. Vitals are normal. Serum LDH is increased. A Coombs test is negative. Two blood smears are shown.
The inheritance pattern of this patient’s condition is the same as which of the following?
α1-antitrypsin deficiency
Cystic fibrosis
Duchenne muscular dystrophy
Hereditary spherocytosis
Sturge-Weber syndrome
