Primary erythromelalgia mainly manifested by hypertensive crisis: A case report and literature review

BACKGROUND: Primary erythrocytic (PEM) is a rare autosomal dominant single gene disease. Most of the changes of gene loci can be found by whole exon gene sequencing, and the clinical symptoms and patient survival can be improved by specific site-to-site drug treatment. The other manifestations of th...

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Detalles Bibliográficos
Autores principales: Feng, Shuo, He, Zhanwen, Que, Liping, Luo, Xiangyang, Liang, Liyang, Li, Dongfang, Qin, Lijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424545/
https://www.ncbi.nlm.nih.gov/pubmed/36052366
http://dx.doi.org/10.3389/fped.2022.796149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424545/
https://www.ncbi.nlm.nih.gov/pubmed/36052366
http://dx.doi.org/10.3389/fped.2022.796149

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