A Hypertrophic Spinal Pachymeningitis Patient With Factor V Leiden (G1691A), MTHFR C677T, MTHFR A1298C, PAI-1 4G-5G, Glycoprotein IIIa L33P Gene Mutations

Hypertrophic pachymeningitis (HP) is a rare clinical entity of diverse etiology, characterized by a chronic inflammation that causes dura thickening. Reports of Idiopathic hypertrophic cranial pachymeningitis (IHCP) were related to infections, trauma, tumors, and rheumatologic conditions. It was fir...

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Detalles Bibliográficos
Autores principales: Civlan, Serkan, Harvey, Cemre, Herek, Duygu, Türkçüer, İbrahim, Sabirli, Ramazan, Pellegrini, Matteo, Koseler, Aylin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634853/
https://www.ncbi.nlm.nih.gov/pubmed/36348907
http://dx.doi.org/10.7759/cureus.29937

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634853/
https://www.ncbi.nlm.nih.gov/pubmed/36348907
http://dx.doi.org/10.7759/cureus.29937

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