Seronegative neuromyelitis optica spectrum disorder in primary familial brain calcification with PDGFB variant

Seronegative neuromyelitis optica spectrum disorder in primary familial brain calcification with PDGFB variant

•This case indicates that the PDGFB variant is associated with PFBC as well as with NMOSD.

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Veröffentlicht in:eNeurologicalSci 2022-06, Vol.27, p.100406-100406, Article 100406
Hauptverfasser: Biyajima, Masahiro, Kobayashi, Yuya, Nakafuji, Kiyoshi, Watanabe, Rie, Tazawa, Koichi, Ishii, Wataru, Satoh, Shunichi, Hoshi, Kenichi, Kurita, Hisaka, Hozumi, Isao, Yahikozawa, Hiroyuki
Format: Artikel
Sprache:eng
Schlagworte:
Blood-brain barrier
Fahr disease
Letters to the Editor
Neuromyelitis optica spectrum disorder
Platelet-derived growth factor subunit B (PDGFB)
Primary familial brain calcification
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Zusammenfassung:•This case indicates that the PDGFB variant is associated with PFBC as well as with NMOSD.
ISSN:2405-6502
2405-6502
DOI:10.1016/j.ensci.2022.100406