医学
MYH7
心脏病学
内科学
心肌病
突变
室致密化不全
基因突变
压实
基因
心力衰竭
遗传学
生物
材料科学
复合材料
基因亚型
作者
Kazım Öztarhan,Beyza Senturk,Özlem Uçar
标识
DOI:10.1017/s1047951122002773
摘要
Abstract Left ventricular non-compaction is a very rare, still unclassified congenital cardiomyopathy. Nine distinct subtypes of functional and anatomical left ventricular non-compaction have been identified. Studies on the prognosis and mortality of subtypes are ongoing. Our study presented the first restrictive subtype left ventricular non-compaction case with family history and MYH7 gene mutation.
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