Cargando…
Concordant nephrotic syndrome in twins with PAX2 and MYO1E mutations
Introduction: The medical literature is scant with reports of twins diagnosed with nephrotic syndrome associated with genetic mutations. Mutations in the protein coding paired box gene 2 (PAX2) and in the non-muscle class I myosin, myosin 1E, (MYO1E) have been implicated in the development of steroi...
Autores principales: | Grossman, Oulimata K., Schretlen, Claire F., Nield, Linda S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dustri-Verlag Dr. Karl Feistle
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097507/ https://www.ncbi.nlm.nih.gov/pubmed/35574290 http://dx.doi.org/10.5414/CNCS110799 |
Ejemplares similares
-
Monozygotic twins concordant for Kleine-Levin syndrome
por: Ueno, Taro, et al.
Publicado: (2012) -
Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in Monozygotic Twins Concordant for Rubinstein-Taybi Syndrome.
por: Akın, Mustafa Ali, et al.
Publicado: (2011) -
Detection of New Translocation in Infant Twins with Concordant ALL and Discordant Outcome
por: Bahoush, Golamreza, et al.
Publicado: (2020) -
Infantile Primary Hyperoxaluria Type 1 Treated With Lumasiran in Twin Males
por: Aldabek, Khaled, et al.
Publicado: (2022) -
Characterization of the promoter region of the bovine SIX1 gene: Roles of MyoD, PAX7, CREB and MyoG
por: Wei, Da-wei, et al.
Publicado: (2017)