Multi-organ hereditary hemorrhagic telangiectasia: A case report

BACKGROUND: Type 2 hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease and is associated with ALK1 gene mutations. Type 2 HHT patients primarily suffer from recurrent bleeding. There is currently no promising treatment. CASE SUMMARY: A 5-year-old Chinese patient (III23)...

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Detalles Bibliográficos
Autores principales: Chen, Ying-Ling, Jiang, Hong-Yue, Li, Dong-Ping, Lin, Jiang, Chen, Yun, Xu, Li-Li, Gao, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600850/
https://www.ncbi.nlm.nih.gov/pubmed/37901025
http://dx.doi.org/10.12998/wjcc.v11.i28.6831

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600850/
https://www.ncbi.nlm.nih.gov/pubmed/37901025
http://dx.doi.org/10.12998/wjcc.v11.i28.6831

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