Factor XIII Deficiency Associated With Noonan Syndrome

Noonan syndrome (NS) is an autosomal dominant disorder with multisystem involvement. NS can be associated with bleeding disorders due to defects in platelet function or coagulation factors and diagnosis can be challenging. Factor XIII (FXIII) deficiency is uncommon in patients with NS. We present a...

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Detalles Bibliográficos
Autores principales: Kharel, Zeni, Katel, Anjan, Neupane, Arun, Panday, Pradumna, Aryal, Madan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076579/
https://www.ncbi.nlm.nih.gov/pubmed/33927952
http://dx.doi.org/10.7759/cureus.14150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076579/
https://www.ncbi.nlm.nih.gov/pubmed/33927952
http://dx.doi.org/10.7759/cureus.14150

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