Ram S P, Noor A R, Ariffin W A, Ariffin N A
Department of Paediatrics, Hospital Universiti Sains Malaysia, Kubang Kerian, Kelantan.
Singapore Med J. 1994 Apr;35(2):205-7.
A 37-week gestation male boy was born to a gravida seven para six mother by spontaneous vertex delivery at home. The baby cried at birth. On day 3 of life, he was admitted for respiratory distress. Physical examination revealed ectrodactyly, thin dry skin, anomalous tear duct with cardiomegaly. X-ray revealed absent radii, cardiomegaly and hemivertebra at L1. Echocardiogram revealed perimembranous type of ventricular septal defect. A diagnosis of Ectodermal Dysplasia Ectrodactyly Clefting Syndrome with ventricular septal defect was made. He was managed conservatively in the nursery. However, he expired on day 27 of life following short spell of fever apnoeic episode due to neonatal sepsis.
一名孕37周的男婴在家中经自然头位分娩出生,其母亲孕7产6。婴儿出生时啼哭。出生后第3天,因呼吸窘迫入院。体格检查发现有缺指(趾)畸形、皮肤薄而干燥、泪道异常伴心脏扩大。X线显示桡骨缺如、心脏扩大及L1半椎体。超声心动图显示膜周型室间隔缺损。诊断为外胚层发育不良缺指(趾)裂综合征合并室间隔缺损。患儿在新生儿重症监护室接受保守治疗。然而,由于新生儿败血症,在出生后第27天,他在短暂的发热呼吸暂停发作后死亡。