Case report: Focal segmental glomerulosclerosis in a pediatric atypical progeroid syndrome

Atypical progeroid syndrome (APS) is a rare type of progeroid syndrome mainly caused by heterozygous missense mutations in the LMNA (MIM 150330) gene. APS has heterogeneous clinical manifestations, and its kidney manifestations, particularly in children, are rarely documented. Here, we report the fi...

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Detalles Bibliográficos
Autores principales: Jang, Seoyun, Ahn, Yo Han, Ko, Jung Min, Ko, Jae Sung, Lim, Sojung, Kang, Hee Gyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660256/
https://www.ncbi.nlm.nih.gov/pubmed/36389384
http://dx.doi.org/10.3389/fped.2022.1032653

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660256/
https://www.ncbi.nlm.nih.gov/pubmed/36389384
http://dx.doi.org/10.3389/fped.2022.1032653

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