A Bejiqi Ramush, J Retkoceri Ragip, Sh Bejiqi Hana
Department of Cardiology, Pediatrics Clinic, University Clinical Centre of Kosova, Prishtina, Kosova.
Acta Inform Med. 2011 Dec;19(4):241-3. doi: 10.5455/aim.2011.19.241-243.
We report a case of a child, with a rare form of the idiopathic hypertrophic cardiomyopathy, associated with mid-cavity obstruction and high intraventricular peak pressure. Cardiomyopathy, diagnosed antenataly, was followed postnataly and, despite of a lot echocardiographic findings - the growing, development and clinical signs are minimal.
我们报告了一例患有罕见形式特发性肥厚型心肌病的儿童病例,该病例伴有中腔梗阻和高心室内峰值压力。心肌病在产前被诊断出来,产后进行了随访,尽管有许多超声心动图检查结果,但生长、发育和临床体征均不明显。