Cargando…
Congenital nephrotic syndrome in a Hispanic Guatemalan newborn associated with a NPHS1 variant: A case report
Congenital nephrotic syndrome (CNS) is an autosomal recessive disorder usually detected in the first 3 months of life when the syndromes effects manifest, including edema and a failure to gain weight. A baby boy was admitted to the Neonatal Intensive Care Unit for prematurity (35 weeks) with unremar...
Autores principales: | Tran, Thu T., Linga, Vijay G., Al-Obaide, Mohammed A.I., Bello-Germino, Daniella, Hoda, Mehar, Adesanya, Olubukunola, Vasylyeva, Tetyana L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652645/ https://www.ncbi.nlm.nih.gov/pubmed/34900253 http://dx.doi.org/10.3892/br.2021.1487 |
Ejemplares similares
-
Possible Correlation between Hypomelanosis of Ito and Wilms' Tumor
por: Bello-Germino, Daniella, et al.
Publicado: (2018) -
Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome
por: Abid, Aiysha, et al.
Publicado: (2018) -
Three Novel Mutations in the NPHS1 Gene in Vietnamese Patients with Congenital Nephrotic Syndrome
por: Nguyen, Thi Kim Lien, et al.
Publicado: (2017) -
Restorative yoga therapy for third-year medical students in pediatrics rotation: Working to improve medical student well-being
por: Thompson, Caroline, et al.
Publicado: (2023) -
Spontaneous remission in a child with an NPHS1-based congenital nephrotic syndrome
por: Espinosa, Laura García, et al.
Publicado: (2022)