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Rapid diagnostic testing of a neonate in a family with hypertrophic cardiomyopathy
Familial hypertrophic cardiomyopathy (HCM) is a common but severe genetic disease. A pregnant woman with familial HCM was referred to our hospital as both the couple and their families were concerned that the baby would later develop HCM. Therefore, we determined the risk of HCM in the neonate. Usin...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
IMR Press
2020-08-01
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| Col·lecció: | Clinical and Experimental Obstetrics & Gynecology |
| Matèries: | |
| Accés en línia: | https://www.imrpress.com/journal/CEOG/47/4/10.31083/j.ceog.2020.04.3433 |
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