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Hemiparesis Revealing a Unique Neurological Hemophagocytic Lymphohistiocytosis in a Patient With Griscelli Syndrome Type 2
Griscelli syndrome (GS) is a rare genetic disorder that encompasses three different subtypes (GS type 1 (GS1), GS type 2 (GS2), and GS type 3 (GS3)), in which isolated neurological manifestations without immune system implications are typically seen in GS1, while neurological involvements in GS2 sho...
Autores principales: | Moueqqit, Othman, Ayad, Ghanam, Benhachem, Madiha, Lahmar, Abdelilah, Ramdani, Hiba, Nadir, Miry, Bensalah, Mohammed, Bennani, Amal, Kamaoui, Imane, Seddik, Rachid, Benajiba, Noufissa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573055/ https://www.ncbi.nlm.nih.gov/pubmed/36259028 http://dx.doi.org/10.7759/cureus.29159 |
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