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...

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Detalles Bibliográficos
Autores principales: Moueqqit, Othman, Ayad, Ghanam, Benhachem, Madiha, Lahmar, Abdelilah, Ramdani, Hiba, Nadir, Miry, Bensalah, Mohammed, Bennani, Amal, Kamaoui, Imane, Seddik, Rachid, Benajiba, Noufissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
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

Internet

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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