Case Report: Preimplantation Genetic Testing and Pregnancy Outcomes in Women With Alport Syndrome

BACKGROUND: Alport syndrome, a monogenic kidney disease, is characterized by progressive hemorrhagic nephritis, sensorineural hearing loss, and ocular abnormalities. Mutations in COL4A5 at Xq22 accounts for 80–85% of X-linked Alport syndrome patients. Three couples were referred to our reproductive...

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Guardat en:
Dades bibliogràfiques
Publicat a:Front Genet
Autors principals: Shi, Wei-Hui, Ye, Mu-Jin, Chen, Song-Chang, Zhang, Jun-Yu, Chen, Yi-Yao, Zhou, Zhi-Yang, Qin, Ning-Xin, Zhou, Xuan-You, Xu, Nai-Xin, Jiang, Zi-Ru, Lin, Jing, Huang, He-Feng, Xu, Chen-Ming
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Genetics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7900551/
https://ncbi.nlm.nih.gov/pubmed/33633790
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.633003
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