Publications by authors named "Taiguang Zhou"
Background: Historically, due to the lack of distinct clinical symptoms, Alport syndrome, a hereditary kidney disease prevalent in children and a leading cause of kidney failure, has often been misdiagnosed as other kidney conditions.
Case Description: This article presents a comprehensive review and analysis of clinical data concerning a child diagnosed with Alport syndrome, where nephrotic syndrome served as the primary manifestation. The male child in this case exhibited symptoms starting at the age of 6, initially diagnosed as nephrotic syndrome.
Case report: Acrodermatitis enteropathica result from a novel gene mutation.
Front Pediatr
November 2022
Article Synopsis
- - A 9-year-old girl with acrodermatitis enteropathica experienced recurrent skin rashes, hair loss, and low zinc levels, which improved significantly with continuous zinc supplementation.
- - Genetic testing revealed she had two specific mutations inherited from her parents, indicating a genetic basis for her condition.
- - The findings from this case could inform further research into acrodermatitis enteropathica and its genetic factors.