Hereditary Hemorrhagic Telangiectasia: Diagnosis and Management
- PMID: 36012936
- PMCID: PMC9410055
- DOI: 10.3390/jcm11164698
Hereditary Hemorrhagic Telangiectasia: Diagnosis and Management
Abstract
Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is a dominantly inheritable rare disease with a prevalence of 1:5000-10,000 inhabitants [...].
Conflict of interest statement
The author declare no conflict of interest.
References
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- Shovlin C.L., Guttmacher A.E., Buscarini E., Faughnan M.E., Hyland R.H., Westermann C.J., Kjeldsen A.D., Plauchu H. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) Am. J. Med. Genet. 2000;91:66–67. doi: 10.1002/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P. - DOI - PubMed
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