Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report
Abstract Background Auriculocondylar syndrome (ACS) is a rare disorder characterized by micrognathia, mandibular condyle hypoplasia, and auricular abnormalities. Only 6 pathogenic variants of GNAI3 have been identified associated with ACS so far. Here, we report a case of prenatal genetic diagnosis...
Saved in:
Main Authors: | Xiaoliang Liu, Wei Sun, Jun Wang, Guoming Chu, Rong He, Bijun Zhang, Yanyan Zhao |
---|---|
Format: | article |
Language: | EN |
Published: |
BMC
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/c2fa9b9572be4ebf84e7b9bbd08a10bf |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review
by: Miroslaw Wielgos, et al.
Published: (2021) -
Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability
by: Chunyan Jin, et al.
Published: (2021) -
Prenatal Diagnosis of Dystrophinopathy and Cytogenetic Analysis in 303 Chinese Families
by: Mengmeng Li, et al.
Published: (2021) -
Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021) -
Decision-making for prenatal genetic screening: how will pregnant women navigate a growing number of aneuploidy and carrier screening options?
by: Ruth M. Farrell, et al.
Published: (2021)