Cited by 105Cleft Lip and Palate ResearchPrenatal Screening and DiagnosticsFetal and Pediatric Neurological Disorders

Maxillary gap at 11–13 weeks’ gestation: Marker of cleft lip and palate

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Chaoui, R., Orosz, G., Heling, K. S., Sarut‐Lopez, A., Nicolaides, K. H.·2015·Ultrasound in Obstetrics & Gynecology

Abstract

Objective: To describe a new sign of cleft lip and palate (CLP), the maxillary gap, which is visible in the mid‐sagittal plane of the fetal face used routinely for measurement of nuchal translucency thickness. Methods: This was a retrospective study of stored images of the mid‐sagittal view of the fetal face at 11–13 weeks' gestation in 86 cases of CLP and 86 normal controls. The images were examined to determine if a maxillary gap was present, in which case its size was measured. Results: In 37 (43.0%) cases of CLP the defect was isolated and in 49 (57.0%) there were additional fetal defects. In the isolated CLP group, the diagnosis of facial cleft was made in the first trimester in nine (24.3%) cases and in the second trimester in 28 (75.7%). In the group with additional defects, the diagnosis of facial cleft was made in the first trimester in 46 (93.9%) cases and in the second trimester in three (6.1%). A maxillary gap was observed in 96% of cases of CLP with additional defects, in 65% of those with isolated CLP and in 7% of normal fetuses. There was a large gap (>1.5 mm) or complete absence of signals from the maxilla in the midline in 69% of cases of CLP with additional defects, in 35% of those with isolated CLP and in none of the normal controls. Conclusions: The maxillary gap is a new simple marker of possible CLP, which could increase the detection rate of CLP, especially in isolated cases. Copyright © 2015 ISUOG. Published by John Wiley & Sons Ltd.

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Crossref · 10.1002/uog.15675

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  • A maxillary gap was seen in 96% of cases with cleft lip and/or palate with additional anomalies, and in 65% the finding was isolated.

    “More specifically, a maxillary gap was seen in 96% of cases with cleft lip and/or palate with additional anomalies, and in 65% the finding was isolated [40].”

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Authors
Chaoui, R., Orosz, G., Heling, K. S., Sarut‐Lopez, A., & Nicolaides, K. H.
Affiliations
  • Zentrum für Pränataldiagnostik (DE)
  • Harris Birthright Research Centre for Fetal Medicine (GB)
  • Center for Prenatal Diagnosis and Human Genetics Berlin Germany
Corresponding author
Chaoui, R.
Venue
Ultrasound in Obstetrics & Gynecology
Publisher
Wiley
Published
2015-11-08
Volume
46
Issue
6
Pages
665-669
ISSN
  • 0960-7692 (ISSN-L)
  • 1469-0705
OpenAlex
W1595369638
Cited by
105
References
0
Citations by year
2026: 7 · 2025: 9 · 2024: 18 · 2023: 14 · 2022: 5 · 2021: 10 · 2020: 10 · 2019: 9 · 2018: 5 · 2017: 11 · 2016: 6 · 2015: 1
FWCI
5.27
Type
journal article
Language
en
Open access
Locations
  • Ultrasound in Obstetrics and Gynecology (publishedVersion)
  • PubMed (publishedVersion)
  • University of Debrecen Electronic Archive (University of Debrecen) (submittedVersion, other-oa)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Cleft Lip and Palate Research
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Screening and Diagnostics
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
Keywords
cleft lip and palate, prenatal diagnosis, first-trimester ultrasound, nuchal translucency, associated congenital anomalies
MeSH terms
Adult, Cleft Lip, Cleft Palate, Female, Fetal Diseases, Gestational Age, Humans, Maxilla, Maxillofacial Development, Pregnancy, Pregnancy Trimester, First, Pregnancy Trimester, Second, Retrospective Studies, Fetal Development, Nuchal Translucency Measurement

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