Lillie Frank Abercrombie Division of Pediatric Cardiology, Texas Children's Hospital, Baylor College of Medicine, 6621 Fannin MC-19345C, Houston, TX 77030, USA.
Heart Fail Clin. 2010 Oct;6(4):445-52, viii. doi: 10.1016/j.hfc.2010.05.005.
Depending on the part of the world one lives in, restrictive cardiomyopathy is either one of the rarest forms of cardiomyopathy in childhood, with no cause usually identified, or it is secondary to a poorly understood disease, endomyocardial fibrosis, that is endemic in some populations. Regardless of the underlying cause, the outcome is poor once symptoms develop. This article reviews the definitions, epidemiology, etiologies, genetics, "overlap" phenotypes, clinical presentation, diagnostic evaluation, outcome, and management of pediatric patients with restrictive cardiomyopathy.
根据人们居住的地区不同,限制型心肌病在儿童心肌病中要么是最罕见的形式之一,通常没有明确的病因,要么是继发于一种病因不明的疾病,即心肌纤维化,这种疾病在某些人群中流行。无论潜在病因如何,一旦出现症状,预后都很差。本文综述了限制型心肌病患儿的定义、流行病学、病因、遗传学、“重叠”表型、临床表现、诊断评估、预后和治疗。