Donnai D, Barrow M
Regional Genetic Service, St Mary's Hospital, Manchester, United Kingdom.
Am J Med Genet. 1993 Oct 1;47(5):679-82. doi: 10.1002/ajmg.1320470518.
We describe unrelated male and female patients with an identical syndrome of diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia. One child had an iris coloboma. After the birth of the first affected child in each family subsequent pregnancies were monitored with ultrasound scan and a further affected fetus was identified in both families. We conclude that this constellation of anomalies represents a distinct, previously unreported syndrome with likely autosomal recessive inheritance.
我们描述了患有相同综合征的非亲缘关系的男性和女性患者,该综合征包括膈疝、脐膨出、眼距过宽、胼胝体发育不全、严重感音神经性耳聋和严重近视。其中一名患儿患有虹膜缺损。在每个家庭中第一个患病儿童出生后,对随后的妊娠进行超声监测,两个家庭均又发现了一名患病胎儿。我们得出结论,这种异常组合代表了一种独特的、以前未报告的综合征,可能为常染色体隐性遗传。