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Fetal spina bifida: What we tell the parents.
Prenatal Diagnosis ( IF 2.7 ) Pub Date : 2020-07-21 , DOI: 10.1002/pd.5802
Lara Gotha 1 , Vagisha Pruthi 1, 2 , Nimrah Abbasi 1, 2 , Abhaya V Kulkarni 2, 3 , Paige Church 4 , James M Drake 2, 3 , Jose C A Carvalho 2, 5 , Yenge Diambomba 2, 6 , Varsha Thakur 2, 7 , Greg Ryan 1, 2 , Tim Van Mieghem 1, 2
Affiliation  

Worldwide, about 150 000 infants are born with spina bifida yearly, making this condition one of the most common fetal central nervous system anomalies compatible with life. Over the last decade, major changes have been introduced in the prenatal diagnosis and management of spina bifida. In this review, we provide a brief summary of the current management of fetal spina bifida and present essential information that should be provided to expecting parents when their fetus has been diagnosed with spina bifida. This information is focused around common parental questions, as encountered in our typical clinical practice, to facilitate knowledge translation.

中文翻译:

胎儿脊柱裂:我们告诉父母的。

在世界范围内,每年约有 150 000 名婴儿出生时患有脊柱裂,这使得这种疾病成为与生活相适应的最常见的胎儿中枢神经系统异常之一。在过去的十年中,脊柱裂的产前诊断和管理发生了重大变化。在这篇综述中,我们简要总结了胎儿脊柱裂的当前管理,并提供了当他们的胎儿被诊断出患有脊柱裂时应向准父母提供的基本信息。这些信息集中在我们典型的临床实践中遇到的常见父母问题,以促进知识翻译。
更新日期:2020-07-21
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