Cargando…
A spectrum of clinical severity of recessive titinopathies in prenatal
Variants in TTN are associated with a broad range of clinical phenotypes, from dominant adult-onset dilated cardiomyopathy to recessive infantile-onset myopathy. However, few foetal cases have been reported for multiple reasons. Next-generation sequencing has facilitated the prenatal identification...
Autores principales: | Qi, Yiming, Ji, Xueqi, Ding, Hongke, Wang, Yunan, Liu, Xin, Zhang, Yan, Yin, Aihua |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907677/ https://www.ncbi.nlm.nih.gov/pubmed/36761691 http://dx.doi.org/10.3389/fgene.2022.1064474 |
Ejemplares similares
-
When NIPT meets WES, prenatal diagnosticians face the dilemma: genetic etiological analysis of 2,328 cases of NT thickening and follow-up of pregnancy outcomes
por: Ji, Xueqi, et al.
Publicado: (2023) -
Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome
por: Qi, Yiming, et al.
Publicado: (2022) -
Novel TTN mutations and muscle imaging characteristics in congenital titinopathy
por: Yu, Meng, et al.
Publicado: (2019) -
Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study
por: Huang, Yanlin, et al.
Publicado: (2023) -
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
por: Oates, Emily C., et al.
Publicado: (2018)