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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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Dades bibliogràfiques
Publicat a:BMC Res Notes
Autors principals: Macêdo, Marina Barguil, Brito, Janaína de Moraes Machado, Macêdo, Plínio da Silva, Brito, José Araújo
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2015
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4434533/
https://ncbi.nlm.nih.gov/pubmed/25928053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1145-5
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