Evaluation of bleeding disorders in patients with Noonan syndrome: a systematic review

BACKGROUND: Noonan syndrome (NS) is an autosomal dominant genetic condition that has a number of clinical features, including bleeding diathesis and a number of hematological abnormalities including clotting factor deficiencies, von Willebrand disease and abnormal platelet count/function. METHODS: W...

Descripción completa

Detalles Bibliográficos
Autores principales: Nugent, Diane J, Romano, Alicia A, Sabharwal, Shreya, Cooper, David L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208935/
https://www.ncbi.nlm.nih.gov/pubmed/30464668
http://dx.doi.org/10.2147/JBM.S164474

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208935/
https://www.ncbi.nlm.nih.gov/pubmed/30464668
http://dx.doi.org/10.2147/JBM.S164474

Ejemplares similares