Hereditary Hemorrhagic Telangiectasia: A Rare Cause of Anemia

Hereditary hemorrhagic telangiectasias (HHT), also known as Osler-Weber-Rendu syndrome, is an uncommon genetic disorder. It is inherited as an autosomal dominant disorder with varying penetrance and expression. The diagnosis of HHT requires the presence of at least three out of four clinical criteri...

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Detalles Bibliográficos
Autores principales: Jan, Waseem, Tameez Ud Din, Asim, Chaudhary, Farooq Mohyud Din, Tameez-ud-din, Ahsan, Nawaz, Faisal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779147/
https://www.ncbi.nlm.nih.gov/pubmed/31602353
http://dx.doi.org/10.7759/cureus.5349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779147/
https://www.ncbi.nlm.nih.gov/pubmed/31602353
http://dx.doi.org/10.7759/cureus.5349

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