AUTHOR=Peng Xia , Xia Li-ping , Zhang Hai-ju , Zhang Jing , Yu Shi-qian , Wang Shun , Xu Yu-ming , Yao Baozhen , Ye Jingping 

TITLE=A Treatable Genetic Disease Caused by CAD Mutation

JOURNAL=Frontiers in Pediatrics

VOLUME=10

YEAR=2022

URL=https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2022.771374

DOI=10.3389/fped.2022.771374

ISSN=2296-2360

ABSTRACT=<p>Type 50 early infantile epileptic encephalopathy, or EIEE-50 for short, is an autosomal recessive genetic disorder resulting from CAD mutations. So far, little has been reported on the disease. In this article, we will discuss the case of a male infant who is 8 years and 5 months old. A whole-exome sequencing of the boy revealed CAD compound heterozygous mutations. He suffered from global developmental delay and regression, refractory epilepsy, and anemia. After his diagnosis, we used uridine treatment and gained encouraging results. In this article, we will analyze our case studies in the context of the literature, so as to improve pediatricians' understanding of the disease.</p>