Prenatally diagnosed microdeletion in the TCOF1 gene in fetal congenital primary Treacher Collins Syndrome
Objective: To study prenatal diagnosis of congenital Treacher Collins syndrome, an etiology of craniofacial abnormalities. Case report: We present a case of fetal craniofacial abnormalities identified by antepartum sonography screening in the third trimester (28 weeks); features of micrognathia, hyp...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Elsevier,
2022-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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