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Article

Clinical and genetic analysis of familial neuromyelitis optica spectrum disorder in Chinese: associated with ubiquitin-specific peptidase USP18 gene variants.

Journal of neurology, neurosurgery, and psychiatry - 1 Dec 2022

Chang Yanyu, Zhou Luyao, Zhong Xiaonan, Shi Ziyan, Sun Xiaobo, Wang Yuge, Li Rui, Long Youming, Zhou Hongyu, Quan Chao, Kermode Allan G, Yu Qingfen, Qiu Wei

Abstract excerpt

BACKGROUND: Familial clustering of neuromyelitis optica spectrum disorder (NMOSD) was present in Chinese. This study was to investigate the clinical characteristics and genetic background of familial NMOSD. METHODS: Through questionnaires in four medical centres in 2016-2020, we identified 10 families with NMOSD aggregation. The statistical differences of clinical characteristics between familial and sporadic...

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PMID: 36376024
DOI: 10.1136/jnnp-2022-329623

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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