Cargando…
Features of Autosomal Recessive Alport Syndrome: A Systematic Review
Alport syndrome (AS) is one of the most frequent hereditary nephritis leading to end-stage renal disease (ESRD). Although X-linked (XLAS) inheritance is the most common form, cases with autosomal recessive inheritance with mutations in COL4A3 or COL4A4 are being increasingly recognized. A systematic...
Autores principales: | Lee, Jiwon M., Nozu, Kandai, Choi, Dae Eun, Kang, Hee Gyung, Ha, II-Soo, Cheong, Hae II |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406612/ https://www.ncbi.nlm.nih.gov/pubmed/30717457 http://dx.doi.org/10.3390/jcm8020178 |
Ejemplares similares
-
A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy
por: Fu, Xue J, et al.
Publicado: (2014) -
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations
por: Savige, Judith, et al.
Publicado: (2016) -
Efficacy of Dapagliflozin in Adult Autosomal Recessive Alport Syndrome
por: Song, Zhuo-ran, et al.
Publicado: (2022) -
COL4A6 is dispensable for autosomal recessive Alport syndrome
por: Murata, Tomohiro, et al.
Publicado: (2016) -
Survival over 2 years of autosomal-recessive renal tubular dysgenesis
por: Kim, Su Yeong, et al.
Publicado: (2012)