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18 November 2022 : Case report  Indonesia

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 ORCID logo1ABCDEFG*, Charity Monica ORCID logo2ABCDEFG, Eko Sulistijono ORCID logo1ACD, Susanto Nugroho ORCID logo3DE, Sony Wicaksono ORCID logo3DE, Setya Mithra Hartiastuti ORCID logo1D

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).

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923