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

Brigitta I.R.V. Corebima; Charity Monica; Eko Sulistijono; Susanto Nugroho; Sony Wicaksono; Setya Mithra Hartiastuti

doi:10.12659/AJCR.937416

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

^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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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

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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

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