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- Title
Reply.
- Authors
Borrell, A.; Paz y Miño, M. F.; Pauta, M.; Meler, E.; Figueras, F.
- Abstract
We thank Drs Chen and Li for the opportunity to clarify further details of our study[1] and agree with the sentiment expressed in the first and final paragraphs of their commentary. Of the 18 cases that consented to exome sequencing and neurodevelopmental assessment, only seven women had undergone prenatal invasive diagnostic testing, with normal karyotyping ( I n i = 2) or chromosome microarray analysis ( I n i = 5) results. To address the first query regarding the number of patients that underwent genetic testing (exome sequencing and copy-number-variation analysis), we refer Drs Chen and Li to our original manuscript, in which we explain that only seven (11%) of the 63 mothers/couples contacted reported a postnatal diagnosis of a genetic syndrome.
- Subjects
LOW birth weight; FETAL growth retardation; AMNIOTIC liquid
- Publication
Ultrasound in Obstetrics & Gynecology, 2023, Vol 62, Issue 3, p450
- ISSN
0960-7692
- Publication type
Article
- DOI
10.1002/uog.26319