Primigravida with Bernard-Soulier Syndrome: a case report

BACKGROUND: Bernard-Soulier Syndrome is a rare congenital bleeding disorder, mainly inherited in an autosomal recessive pattern. It is characterized by a genetic defect on one of the four genes encoding the subunits of the transmembrane protein complex GPIb-V-IX, physiologically expressed only in pl...

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Detalles Bibliográficos
Autores principales: Macêdo, Marina Barguil, Brito, Janaína de Moraes Machado, Macêdo, Plínio da Silva, Brito, José Araújo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434533/
https://www.ncbi.nlm.nih.gov/pubmed/25928053
http://dx.doi.org/10.1186/s13104-015-1145-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434533/
https://www.ncbi.nlm.nih.gov/pubmed/25928053
http://dx.doi.org/10.1186/s13104-015-1145-5

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