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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Main Authors: Seoyun Jang (Author), Yo Han Ahn (Author), Jung Min Ko (Author), Jae Sung Ko (Author), Sojung Lim (Author), Hee Gyung Kang (Author)
Format: Book
Published: Frontiers Media S.A., 2022-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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