Co‐occurrence of glial fibrillary acidic protein astrocytopathy in a patient with Leber's hereditary optic neuropathy due to DNAJC30 mutations

Leber's hereditary optic neuropathy (LHON) is a mitochondrial disease characterized by visual loss, and rarely associated with extraocular manifestations including multiple sclerosis‐like lesions. The association of LHON and neuromyelitis optica spectrum disorders has rarely been reported. Here...

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Veröffentlicht in:	European journal of neurology 2024-09, Vol.31 (9), p.e16344-n/a
Hauptverfasser:	Giannoccaro, Maria Pia, Morelli, Luana, Ricciardiello, Fortuna, Donadio, Vincenzo, Bartiromo, Fiorina, Tonon, Caterina, Carbonelli, Michele, Amore, Giulia, Carelli, Valerio, Liguori, Rocco, La Morgia, Chiara
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Area postrema area postrema syndrome Astrocytes - metabolism Astrocytes - pathology Case Report Female GFAP antibodies GFAP astrocytopathy Glial fibrillary acidic protein Glial Fibrillary Acidic Protein - genetics HSP40 Heat-Shock Proteins - genetics Humans Leber's hereditary optic neuropathy Leber's optic atrophy Male Multiple sclerosis Mutation Neurogenetics Neuromyelitis neuromyelitis optica Neuronal-glial interactions NMOSD Optic Atrophy, Hereditary, Leber - complications Optic Atrophy, Hereditary, Leber - genetics Optic neuropathy Proteins
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