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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: H. Ueda, T. Miyamoto, Y. Tsurusaki, G. Minase, N. Matsumoto, K. Sengoku
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: IMR Press 2020-08-01
Sarja:Clinical and Experimental Obstetrics & Gynecology
Aiheet:
early diagnosis
hypertrophic cardiomyopathy
mutation
myh7
whole-exome sequencing
Linkit:https://www.imrpress.com/journal/CEOG/47/4/10.31083/j.ceog.2020.04.3433
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