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Targeting under-diagnosis in hereditary hemorrhagic telangiectasia: a model approach for rare diseases?
BACKGROUND: Hereditary hemorrhagic telangiectasia (HHT), a rare autosomal dominant disease, is considered under-diagnosed. Our primary objective was to provide evidence of under-diagnosis of HHT in a North American population. We hypothesized that variation would exist in the diagnosed prevalence (D...
Gardado en:
| Publicado en: | Orphanet J Rare Dis |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4222286/ https://ncbi.nlm.nih.gov/pubmed/25060326 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-014-0115-7 |
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