Hemophagocytic lymphohistiocytosis: A rare cause of recurrent encephalopathy

We report an unusual case of recurrent encephalopathy due to acquired hemophagocytic lymphohistiocytosis (HLH) in a patient with propionic acidemia (PA). PA is an inherited metabolic disorder in which patients often present with encephalopathy and pancytopenia during metabolic decompensation. Howeve...

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Veröffentlicht in:Intractable Rare Dis Res
Hauptverfasser: Sulaiman, Raashda Ainuddin, Shaheen, Marwan Yassin, Al-Zaidan, Hamad, Al-Hassnan, Zuhair, Al-Sayed, Moeenaldeen, Rahbeeni, Zuhair, Bakshi, Nasir Ahmed, Kaya, Namik, Aldosary, Mazhor, Al-Owain, Mohammed
Format: Artigo
Sprache:Inglês
Veröffentlicht: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2016
Schlagworte:
Case Report
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4995419/
https://ncbi.nlm.nih.gov/pubmed/27672548
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2016.01018
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