Encephalitis Unraveled: The Unlikely Encounter of Sickle Cell Disease and Cerebral Malaria in a Teenager

Sickle-cell disease (SCD) is a group of inherited blood disorders in which a mutation in the β-globin (HBB) gene causes red blood cells to produce abnormal hemoglobin, known as Hb S. SCD is characterized by an autosomal-recessive pattern of inheritance, implying that for a child to manifest the cond...

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Auteurs principaux:	Christer Ruff, Leonie Zerweck, Andrea Bevot, Jonathan Remppis, Benjamin Bender, Ulrike Ernemann, Georg Gohla
Format:	Artigo
Langue:	Inglês
Publié:	MDPI AG 2025-06-01
Collection:	Diagnostics
Sujets:	central nervous system (CNS) cerebral malaria hemoglobin (HB) magnetic resonance imaging (MRI) sickle cell disease (SCD)
Accès en ligne:	https://www.mdpi.com/2075-4418/15/12/1470
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