Owren's Disease: A Rare Deficiency

Factor V deficiency is a rare bleeding disorder, which may be due to acquired inhibitors or biallelic mutations. Factor V deficiency due to homozygous or compound heterozygous mutation (also known as Owren's disease or parahemophilia) has an estimated prevalence of one in one million people. A...

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Detalles Bibliográficos
Autores principales: Ehtisham, Madiha, Shafiq, Muhammad A, Shafique, Muhammad, Mumtaz, Hassan, Shahzad, Muhammad Naveed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Emergency Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427937/
https://www.ncbi.nlm.nih.gov/pubmed/34522525
http://dx.doi.org/10.7759/cureus.17047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427937/
https://www.ncbi.nlm.nih.gov/pubmed/34522525
http://dx.doi.org/10.7759/cureus.17047

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