Pass R F, Stagno S, Myers G J, Alford C A
Pediatrics. 1980 Nov;66(5):758-62.
Thirty-four patients with congenital cytomegalovirus infection who were symptomatic as newborns were followed in a special clinic providing periodic medical and visual examinations as well as psychometric testing and audiometry. All patients had symptoms of congenital infection by 2 weeks of age, and 31 of 34 had virus isolated from urine within the first month of life. Age at latest follow-up varied from 9 months to 14 years with a mean of about 4 years. Ten patients died and 23 surviving patients had adequate follow-up examinations; all but two had evidence of central nervous system or auditory handicaps. Microcephaly was present in 16 (70%), mental retardation in 14 (61%), hearing loss in seven (30%), neuromuscular disorders in eight (35%), and chorioretinitis or optic atrophy in five (22%). Children with symptomatic congenital cytomegalovirus infection are at very high risk for handicaps that will significantly impair development.
34例先天性巨细胞病毒感染且出生时即有症状的患儿在一家特殊诊所接受随访,该诊所提供定期的医学检查、视力检查、心理测试和听力测定。所有患儿在2周龄时均出现先天性感染症状,34例中有31例在出生后第一个月内尿液中分离出病毒。最后一次随访时的年龄从9个月至14岁不等,平均约4岁。10例患儿死亡,23例存活患儿接受了充分的随访检查;除2例患儿外,所有患儿均有中枢神经系统或听觉障碍的证据。16例(70%)有小头畸形,14例(61%)有智力发育迟缓,7例(30%)有听力损失,8例(35%)有神经肌肉疾病,5例(22%)有脉络膜视网膜炎或视神经萎缩。有症状的先天性巨细胞病毒感染患儿出现严重影响发育的障碍的风险非常高。