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
1ABCDEFG*, Charity Monica 2ABCDEFG, Eko Sulistijono 1ACD, Susanto Nugroho 3DE, Sony Wicaksono 3DE, Setya Mithra Hartiastuti 1D
DOI: 10.12659/AJCR.937416
Am J Case Rep 2022; 23:e937416
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