Syndrome de Scott et grossesse: à propos d’un cas

Scott´s syndrome is a rare congenital thrombopathy with an autosomal recessive inheritance pattern. The purpose of our study is to report the case of a parturient woman with Scott´s syndrome secondary to a mutation of the ANO6 gene never described in the literature. After 3 bleeding episodes, in par...

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Detalles Bibliográficos
Autores principales: Bouchaib, Allae Eddine, Balde, Mamadou Alpha, Babahabib, Abdellah, Elhassani, Moulay El Mehdi, Kouach, Jaouad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349627/
https://www.ncbi.nlm.nih.gov/pubmed/37455884
http://dx.doi.org/10.11604/pamj.2023.44.151.38361

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349627/
https://www.ncbi.nlm.nih.gov/pubmed/37455884
http://dx.doi.org/10.11604/pamj.2023.44.151.38361

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