18 November 2022
: Case report
A 6-Day-Old Male Infant with Severe Hyperbilirubinemia Diagnosed with Hereditary Spherocytosis at a Tertiary Hospital in East Java, Indonesia: A Diagnostic and Management Challenge in a Developing Country
Challenging differential diagnosis, Unusual setting of medical care, Rare disease
Brigitta I.R.V. Corebima





DOI: 10.12659/AJCR.937416
Am J Case Rep 2022; 23:e937416
Figure 1. The patient’s blood smear. The blood smear showed some spherocytes small erythrocytes lacking central pallor (blue arrows).