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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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Main Authors: H. Ueda, T. Miyamoto, Y. Tsurusaki, G. Minase, N. Matsumoto, K. Sengoku
Formato: Artigo
Idioma:Inglês
Publicado: IMR Press 2020-08-01
Series:Clinical and Experimental Obstetrics & Gynecology
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Acceso en liña:https://www.imrpress.com/journal/CEOG/47/4/10.31083/j.ceog.2020.04.3433
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