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...

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Detalles Bibliográficos
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:
Articles
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

Internet

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

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