Open AccessIdentification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome
Author(s) -
Liu Jing,
Lin Pengsiyuan,
Pang Jialun,
Jia Zhengjun,
Peng Ying,
Xi Hui,
Wu Lingqian,
Li Zhuo,
Wang Hua
Publication year - 2020
Publication title -
molecular genetics and genomic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 29
ISSN - 2324-9269
DOI - 10.1002/mgg3.1313
Subject(s) - treacher collins syndrome , multiplex ligation dependent probe amplification , prenatal diagnosis , genetics , craniofacial , exon , medicine , exome sequencing , genetic counseling , fetus , craniofacial abnormality , biology , gene , mutation , pregnancy
Background Treacher Collins syndrome (TCS) is the most common mandibulofacial dysostosis with an autosomal dominant or rarely recessive manner of inheritance. It is still challenging to make a definite diagnosis for affected fetuses with TCS only depending on the ultrasound screening. Genetic tests can contribute to the accurate diagnosis for those prenatal cases. Methods Targeted exome sequencing was performed in a fetus of a Chinese family, who presenting an abnormal facial appearance by prenatal 2D and 3D ultrasound screening, including micrognathia, nasal bridge pit, and abnormal auricle. The result was validated with multiplex ligation‐dependent probe amplification (MLPA) and real‐time quantitative PCR (qPCR). Results A novel 2–6 exons deletion of TCOF1 gene was identified and confirmed by the MLPA and qPCR in the fetus, which was inherited from the affected father with similar facial anomalies. Conclusion The heterozygous deletion of 2–6 exons in TCOF1 results in the TCS of this Chinese family. Our findings not only enlarge the spectrum of mutations in TCOF1 gene, but also highlight the values of combination of ultrasound and genetics tests in diagnosis of craniofacial malformation‐related diseases during perinatal period.