دورية أكاديمية
أعرض في EDS

Compound heterozygous variants in DYNC2H1 in a foetus with type III short rib-polydactyly syndrome and situs inversus totalis.

التفاصيل البيبلوغرافية
العنوان: Compound heterozygous variants in DYNC2H1 in a foetus with type III short rib-polydactyly syndrome and situs inversus totalis.
المؤلفون: Cheng C; Department of Ultrasonography, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430070, China., Li X; College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China., Zhao S; Department of Ultrasonography, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430070, China., Feng Q; Department of Ultrasonography, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430070, China., Ren X; College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China., Chen X; Department of Ultrasonography, Maternal and Child Health Hospital of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430070, China. 928339431@qq.com.
المصدر: BMC medical genomics [BMC Med Genomics] 2022 Mar 12; Vol. 15 (1), pp. 55. Date of Electronic Publication: 2022 Mar 12.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE
أسماء مطبوعة: Original Publication: London : BioMed Central
مواضيع طبية MeSH: Dextrocardia* , Polydactyly* , Short Rib-Polydactyly Syndrome*/diagnostic imaging , Short Rib-Polydactyly Syndrome*/genetics , Situs Inversus*/diagnostic imaging , Situs Inversus*/genetics, Cytoplasmic Dyneins/genetics ; Female ; Fetus/diagnostic imaging ; Humans ; Pregnancy
مستخلص: Background: Short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3, OMIM: 613091) is an autosomal recessive disorder. SRTD3 presents clinically with a narrow thorax, short ribs, shortened tubular bones, and acetabular roof abnormalities. Clinical signs of SRTD3 vary among individuals. Pathogenic variants of DYNC2H1 (OMIM: 603297) have been reported to cause SRTD3.
Methods: We performed a detailed clinical prenatal sonographic characterization of a foetus with SRTD3. Trio whole-exome sequencing was used to identify causative variants in the family. The identified variants in the families were validated by Sanger sequencing and mass spectrometry. Multiple computational tools were used to predict the harmfulness of the two variants. A minigene splicing assay was carried out to evaluate the impact of the splice-site variant.
Results: We evaluated prenatal sonographic images of the foetus with SRTD3, including abnormal rib curvature, narrow thorax, bilateral hypoplastic lungs, bilateral polydactyly, syndactyly, and foetal visceral situs inversus with mirror-image dextrocardia. We revealed novel compound variants of DYNC2H1 (NM_001377.3:c.11483T > G (p.Ile3828Arg) and c.2106 + 3A > T). Various statistical methods predicted that the variants would cause harmful effects on genes or gene products. The minigene assay findings suggested that c.2106 + 3A > T caused the skipping over exon 14, producing an exon 14 loss in the protein.
Conclusion: This study identified a foetus with SRTD3 with situs inversus totalis with mirror-image dextrocardia in a Chinese family, revealing two novel compound heterozygous dynein cytoplasmic 2 heavy chain 1 (DYNC2H1) variants, expanding the phenotypic spectrum of SRTD3. The minigene study of c.2106 + 3A > T was predicted to cause an inframe exclusion of exon 14, which was predicted to have important molecular functions. Our findings strongly supported the use of WES in prenatal diagnosis and helped to understand the correlation of genotype and phenotypes of DYNC2H1. The specific sonographic findings and the molecular diagnosis helped add experience to further our expertise in prenatal counselling for SRTD3.
(© 2022. The Author(s).)
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المشرفين على المادة: 0 (DYNC2H1 protein, human)
EC 3.6.4.2 (Cytoplasmic Dyneins)
SCR Disease Name: Short rib-polydactyly syndrome, Verma-Naumoff type
تواريخ الأحداث: Date Created: 20220312 Date Completed: 20220425 Latest Revision: 20220425
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC8917749
DOI: 10.1186/s12920-022-01205-z
PMID: 35277174
قاعدة البيانات: MEDLINE
الوصف
تدمد:1755-8794
DOI:10.1186/s12920-022-01205-z