Cargando…
Novel variants of NEK9 associated with neonatal arthrogryposis: Two case reports and a literature review
Objective: Pathogenic variants in NEK9 (MIM: 609798) have been identified in patients with lethal congenital contracture syndrome 10 (OMIM: 617022) and arthrogryposis, Perthes disease, and upward gaze palsy (APUG and OMIM: 614262). The shared core phenotype is multiple joint contractures or arthrogr...
Autores principales: | Liu, Fang, Dai, Liying, Li, Zhi, Yin’s, Xiaowei |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879004/ https://www.ncbi.nlm.nih.gov/pubmed/36712877 http://dx.doi.org/10.3389/fgene.2022.989215 |
Ejemplares similares
-
Case report: identification of one frameshift variant and two in cis non-canonical splice variants of NEB gene in prenatal arthrogryposis
por: Liu, Yuefang, et al.
Publicado: (2023) -
Case Report: Novel Biallelic Null Variants of SMPD4 Confirm Its Involvement in Neurodevelopmental Disorder With Microcephaly, Arthrogryposis, and Structural Brain Anomalies
por: Ji, Weigang, et al.
Publicado: (2022) -
Mild Phenotype of Arthrogryposis, Renal Dysfunction, and Cholestasis Syndrome 1 Caused by a Novel VPS33B Variant
por: Linhares, Natália Duarte, et al.
Publicado: (2022) -
Novel Neonatal Variants of the Carbamoyl Phosphate Synthetase 1 Deficiency: Two Case Reports and Review of Literature
por: Yan, Beibei, et al.
Publicado: (2019) -
Novel Consensus Splice Site Pathogenic Variation in THOC2 Gene Leads to Recurrent Arthrogryposis Multiplex Congenita Phenotype: A Case Report
por: Tamhankar, Vasundhara, et al.
Publicado: (2021)