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

BackgroundPrimary 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 this...

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Asıl Yazarlar: Shuo Feng (Yazar), Zhanwen He (Yazar), Liping Que (Yazar), Xiangyang Luo (Yazar), Liyang Liang (Yazar), Dongfang Li (Yazar), Lijun Qin (Yazar)
Materyal Türü: Kitap
Baskı/Yayın Bilgisi: Frontiers Media S.A., 2022-08-01T00:00:00Z.
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