产前诊断孤立性脑室肿大、小头畸形和脑膨出的临床随访。

Fetal therapy Pub Date : 1989-01-01 DOI:10.1159/000263390
R D Wilson, D Hitchman, B K Wittman
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引用次数: 13

摘要

本研究通过不列颠哥伦比亚大学格雷斯医院超声科对约22000例连续患者的孤立性脑室肿大(无脊柱裂)、脑膨出和小头畸形进行回顾性分析,共发现17例孤立性脑室肿大、16例小头畸形和6例脑膨出。孤立性脑室肿大和脑膨出的产前诊断准确,而小头畸形的产前诊断不一致。孤立性脑室肿大患者有颅异常家族史阳性的占24%。脑室肿大胎儿的预后很难预测,但严重的脑室肿大通常预后较差,而轻度或中度脑室肿大则导致正常发育或轻度发育迟缓。建议对所有中枢神经系统病变患者进行染色体分析,建议对脑室肿大和小头畸形患者进行病毒检查。
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Clinical follow-up of prenatally diagnosed isolated ventriculomegaly, microcephaly and encephalocele.

This retrospective review identified all cases of isolated ventriculomegaly (without spina bifida), encephalocele and microcephaly in approximately 22,000 consecutive patients through the Ultrasound Department at the University of British Columbia, Grace Hospital. 17 cases of isolated ventriculomegaly, 16 cases of microcephaly and 6 cases of encephalocele were identified. Isolated ventriculomegaly and encephalocele were accurately diagnosed prenatally while microcephaly was not consistently identified prenatally. Patients with isolated ventriculomegaly had a positive family history for cranial abnormalities in 24%. The prognosis is difficult to predict for fetuses with ventriculomegaly, but severe ventriculomegaly generally produced a poor outcome while mild or moderate ventriculomegaly resulted in normal development or marginal developmental delay. Chromosome analysis is recommended in all patients with central nervous system lesions and viral studies are recommended with ventriculomegaly and microcephaly.

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