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

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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Bibliographic Details
Main Authors: Seoyun Jang, Yo Han Ahn, Jung Min Ko, Jae Sung Ko, Sojung Lim, Hee Gyung Kang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Pediatrics
Subjects:
focal segmental glomerular sclerosis (FSGS)
atypical progeroid syndrome
lipodystrophy
LMNA
TGF - β1
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2022.1032653/full

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