Expanding the clinical spectrum of 19p13.3 microduplication syndrome: a case report highlighting nephrotic syndrome and literature review

Expanding the clinical spectrum of 19p13.3 microduplication syndrome: a case report highlighting nephrotic syndrome and literature review

Abstract Background Common clinical findings in patients with 19p13.3 duplication include intrauterine growth restriction, intellectual disability, developmental delay, microcephaly, and distinctive facial features. In this study, we report the case of a patient with 19p13.3 microduplication and nov...

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Bibliographic Details
Main Authors: Wenjie Sun, Hong Yan, Mengxin Sun, Jie Wang, Kunxia Li
Format: Article
Language:English
Published: BMC 2025-01-01
Series:BMC Pediatrics
Subjects:
Duplication
19p13.3
Nephrotic syndrome
Chromosome microarray analysis
Online Access:https://doi.org/10.1186/s12887-025-05394-1
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