VHL syndrome without clear family history: A rare case report and literature review of Chinese patients

OBJECTIVE: To analyze the clinical manifestations and imaging features of a hospitalized patient with intermittent headache who was finally diagnosed with von Hippel–Lindau (VHL) syndrome and to perform whole-exon gene detection to improve the understanding of the diagnosis and treatment strategies...

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Detalles Bibliográficos
Autores principales: Li, Yaheng, Xin, Xiaohong, Song, Wenzhu, Zhang, Xuan, Chen, Shengli, Wang, Qian, Li, Aizhong, Li, Yafeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618664/
https://www.ncbi.nlm.nih.gov/pubmed/36324386
http://dx.doi.org/10.3389/fneur.2022.951054

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618664/
https://www.ncbi.nlm.nih.gov/pubmed/36324386
http://dx.doi.org/10.3389/fneur.2022.951054

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