Cunniff C, Jones K L, Jones M C
Department of Pediatrics, University of California, San Diego.
J Pediatr. 1990 Feb;116(2):258-61. doi: 10.1016/s0022-3476(05)82884-7.
The medical records of 102 live-born children with a congenital diaphragmatic defect were reviewed to determine the frequency and nature of underlying chromosomal, genetic, and nongenetic patterns of malformation. Overall, 40 children (39%) had a major nonpulmonary malformation, and 14 of these children (14%) had a previously recognized pattern of malformation. A group of 18 children (18%) with cardiac anomalies had an increased mortality rate in comparison with those children without cardiac defects (72% vs 38%). The frequency and severity of nonpulmonary abnormalities in children with congenital diaphragmatic defects suggest that examination of affected children should include cardiac evaluation, a karyotype when the defect is one feature of a broader pattern of altered development, and a careful evaluation for minor anomalies, which may provide clues to an overall diagnosis.
回顾了102例先天性膈疝活产儿的病历,以确定潜在的染色体、遗传和非遗传畸形模式的频率和性质。总体而言,40名儿童(39%)有主要的非肺部畸形,其中14名儿童(14%)有先前已确认的畸形模式。与无心脏缺陷的儿童相比,一组18名有心脏异常的儿童(18%)死亡率更高(72%对38%)。先天性膈疝患儿非肺部异常的频率和严重程度表明,对受影响儿童的检查应包括心脏评估;当缺陷是更广泛发育改变模式的一个特征时,应进行核型分析;并仔细评估轻微异常,这可能为整体诊断提供线索。