Hereditární hemoragická teleangiektázie (syndrom Osler-Weber-Rendu) Díl I. Patofyziologie, klinické příznaky a doporučený skrínink cévních malformací
[Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations]
Language Czech Country Czech Republic Media print
Document type Journal Article
PubMed
35459376
PII: 130094
- Keywords
- arteriovenous malformation, arteriovenous malformations, hereditary haemorrhagic telangiectasia, hereditary hemorrhagic teleangiectasia,
- MeSH
- Arteriovenous Malformations * complications diagnosis genetics MeSH
- Telangiectasia, Hereditary Hemorrhagic * complications diagnosis genetics MeSH
- Humans MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes abnormal blood vessel formation. Patients with HHT may have telangiectasias and later may develop arteriovenous malformations in various organs. Pacients suffer from many complications caused by the malformations and therefore by patients with HHT must by performed screening of this arteriovenous malformations. Optimal treatment of this malformations is best delivered throught a multidisciplinary approach. Farmacological treatment is described in next paper.
