Myosin Heavy Chain 9 (MYH9)-Related Congenital Macrothrombocytopenia

Myosin heavy chain 9 (MYH9)-related hereditary macrothrombocytopenia is caused by mutation of the MYH9 gene encoding the heavy chain A of non-muscle myosin of class II. We present a case that emphasizes the importance of awareness of rare disorders which could potentially avoid over-investigation, e...

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Detalles Bibliográficos
Autores principales: Thurlapati, Aswani, Guntupalli, Srinandan, Mansour, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419368/
https://www.ncbi.nlm.nih.gov/pubmed/34527454
http://dx.doi.org/10.7759/cureus.16964

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419368/
https://www.ncbi.nlm.nih.gov/pubmed/34527454
http://dx.doi.org/10.7759/cureus.16964

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