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

Patient: Male, 6-day-old Final Diagnosis: Hereditary spherocytosis Symptoms: Severe hyperbilirubinemia Medication:— Clinical Procedure: Intensive phototherapy Specialty: Hematology • Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Hereditary spherocytosis (HS) is an autosomal dominant...

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Detalles Bibliográficos
Autores principales: Corebima, Brigitta I.R.V., Monica, Charity, Sulistijono, Eko, Nugroho, Susanto, Wicaksono, Sony, Hartiastuti, Setya Mithra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679984/
https://www.ncbi.nlm.nih.gov/pubmed/36399434
http://dx.doi.org/10.12659/AJCR.937416

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