Postnatal genetic and neurodevelopmental assessment in infants born at term with severely low birth weight of non-placental origin

dc.contributor.author
Paz y Miño, Fernanda
dc.contributor.author
Pauta, Montse
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Meler Barrabés, Eva
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Matas, Isabel
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Mazarico Gallego, Edurne
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Camacho, Araceli
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Segura, Maria
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Figueras, Francesc
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Borrell, Antoni
dc.date.issued
2024-12-23T15:03:25Z
dc.date.issued
2024-12-23T15:03:25Z
dc.date.issued
2023-09-01
dc.date.issued
2024-12-23T15:03:25Z
dc.identifier
0960-7692
dc.identifier
https://hdl.handle.net/2445/217247
dc.identifier
751749
dc.identifier
36840980
dc.description.abstract
Objective: To determine the frequency of genetic syndromes and childhood neurodevelopmental impairment in non-malformed infants born at term with severely low birth weight and no evidence of placental insufficiency. Methods: This case series was constructed from the data of infants delivered at term between 2013 and 2018 with severely low birth weight, defined as birth weight more than 2.5 SD below the mean, with normal maternal and fetal Doppler (umbilical artery, fetal middle cerebral artery, cerebroplacental ratio and uterine artery) and no maternal hypertensive disorder during pregnancy or fetal structural anomaly on prenatal ultrasound examination. Clinical exome sequencing and copy number variation (CNV) analysis were performed using DNA extracted from the children's saliva. Cognitive and psychomotor development was evaluated using the Bayley Scales of Infant and Toddler Development, 3rd edition or the Wechsler Intelligence Scale for Children, 5th edition tests, according to the child's age at testing. Results: Among the 36 405 infants born within the study period, 274 (0.75%) had a birth weight below -2.5 SD, of whom 98 met the inclusion criteria. Among the 63 families contacted, seven (11%) reported a postnatal diagnosis of a genetic syndrome and a further 18 consented to participate in the study. Median gestational age at delivery was 38.0 (interquartile range (IQR), 37.3-38.5) weeks and median birth weight was 2020 (IQR, 1908-2248) g. All 18 children showed a normal result on clinical exome sequencing and CNV analysis, but six (33%) obtained a low score on neurodevelopmental testing. Conclusion: Non-malformed severely small term infants with no clinical or Doppler signs of placental insufficiency present a high rate of genetic syndromes and neurodevelopmental impairment during childhood. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
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8 p.
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application/pdf
dc.language
eng
dc.publisher
John Wiley & Sons
dc.relation
Reproducció del document publicat a: https://doi.org/10.1002/uog.26188
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Ultrasound in Obstetrics & Gynecology, 2023, vol. 62, num.3, p. 361-368
dc.relation
https://doi.org/10.1002/uog.26188
dc.rights
cc-by-nc-nd (c) Paz y Miño, Fernanda et al., 2023
dc.rights
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)
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Malalties hereditàries
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Diagnòstic prenatal
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Infants nadons
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Desenvolupament infantil
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Neurologia dels nadons
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Genetic diseases
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Prenatal diagnosis
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Newborn infants
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Child development
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Neonatal neurology
dc.title
Postnatal genetic and neurodevelopmental assessment in infants born at term with severely low birth weight of non-placental origin
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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