A Child with Paroxysmal Extreme Pain Disorder and Erythromelalgia: Challenges in Hypertension Treatment
Paroxysmal extreme pain disorder (PEPD) and inherited erythromelalgia (IEM) are two distinct syndromes caused by pathogenic mutations in the SCN9A gene. Still, they can be part of a clinical continuum manifesting in the same patient. The main clinical characteristics are painful attacks accompani...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Sestre Milosrdnice University hospital, Institute of Clinical Medical Research
2025-01-01
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| Col·lecció: | Acta Clinica Croatica |
| Matèries: | |
| Accés en línia: | https://hrcak.srce.hr/file/497757 |
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