Cargando…
Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by IL2RG Gene Variant
Preimplantation genetic testing (PGT) has been increasingly used to prevent rare inherited diseases. In this study, we report a case where PGT was used to prevent the transmission of disease-caused variant in a SCID-X1 (OMIM:300400) family. SCID-X1 is an X-linked recessive inherited disease whose ma...
Autores principales: | Ren, Jun, Peng, Cuiting, Zhou, Fan, Li, Yutong, Keqie, Yuezhi, Chen, Han, Zhu, Hongmei, Chen, Xinlian, Liu, Shanling |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198258/ https://www.ncbi.nlm.nih.gov/pubmed/35719382 http://dx.doi.org/10.3389/fgene.2022.926060 |
Ejemplares similares
-
Case report: Optical genome mapping revealed double rearrangements in a male undergoing preimplantation genetic testing
por: Ren, Jun, et al.
Publicado: (2023) -
A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation
por: Peng, Cuiting, et al.
Publicado: (2023) -
Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1
por: Chen, Songchang, et al.
Publicado: (2020) -
Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality
por: Zhang, Manyu, et al.
Publicado: (2021) -
Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of SPTB
por: Tian, Yafei, et al.
Publicado: (2023)