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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...

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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

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