医学
肥厚性心肌病
支气管肺炎
心肌病
子宫内
儿科
心力衰竭
心肌肥大
心脏病学
肌肉肥大
胎儿
怀孕
遗传学
生物
作者
Francesco Lupariello,Giancarlo Di Vella,Giovanni Botta
标识
DOI:10.1080/15513815.2019.1655820
摘要
Background: Hypertrophic cardiomyopathy is characterized by intrinsic myocardial hypertrophy that is not consequent to hemodynamic stimuli. Infantile hypertrophic cardiomyopathy (<1 year of age) has a frequency of about 3.6 per 1 million children, is usually diagnosed in utero, at birth, or in the first months of life. The most common outcome of this form is heart failure that may result in the death of the child. Case Report: We present an 11-month old infant with hypertrophic cardiomyopathy, complicated by terminal bronchopneumonia, without the typical clinical signs/symptoms in which the diagnosis was made only after postmortem examination. Conclusion: The present report depicts that IHCM may present with the unexpected death of an infant.
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