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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| 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 |