2017
DOI: 10.1002/jcu.22535
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Prenatal 3D sonography of an isolated lateral facial cleft

Abstract: Lateral facial cleft is a rare congenital anomaly, but all affected infants require surgery under general anesthesia. Conventional 2-dimensional coronal view of the face, which is typically used for identification of facial clefts, has limitations with regard to detection of this anomaly. We describe a case of prenatal diagnosis of isolated lateral facial cleft made with 3D sonography and highlight the importance of this tool in the diagnosis of this rare facial deformity.

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Cited by 3 publications
(5 citation statements)
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“…Genetic investigations were performed in six cases, which did not reveal any chromosomal abnormalities. 5,6,10,[12][13][14] The noteworthy feature in our case was macrostomia with bilateral diastasis extending to the preauricular area. These structural abnormalities are considered to be associated with restricted movement of the temporomandibular joint (TMJ).…”
Section: Discussionmentioning
confidence: 56%
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“…Genetic investigations were performed in six cases, which did not reveal any chromosomal abnormalities. 5,6,10,[12][13][14] The noteworthy feature in our case was macrostomia with bilateral diastasis extending to the preauricular area. These structural abnormalities are considered to be associated with restricted movement of the temporomandibular joint (TMJ).…”
Section: Discussionmentioning
confidence: 56%
“…9,11 Intra-uterine synechiae was observed in two cases that was later confirmed during caesarean section. 5,6 However, no clear evidence of amniotic bands was present either at ultrasound or postnatal examination of the neonate and placentas in both cases. Genetic investigations were performed in six cases, which did not reveal any chromosomal abnormalities.…”
Section: Discussionmentioning
confidence: 85%
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“…Including the current report, a total of 11 cases with a lateral facial cleft have been diagnosed prenatally, all of which were initially screened or diagnosed by ultrasonography, which is a routine prenatal screening examination for the fetus. Among the reported cases, the average age of mothers was 31.5 years, and their obstetrical circumstances are listed below[ 12 - 14 ] (Table 1 ). The fetuses were initially suspected to have facial malformations between 21 wk and 33 wk of gestation, and six cases were diagnosed within the mid-trimester.…”
Section: Discussionmentioning
confidence: 99%