Case Report
Copyright ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Mar 6, 2022; 10(7): 2330-2335
Published online Mar 6, 2022. doi: 10.12998/wjcc.v10.i7.2330
Novel mutations of the Alström syndrome 1 gene in an infant with dilated cardiomyopathy: A case report
Ping Jiang, Liang Xiao, Yuan Guo, Rong Hu, Bo-Yi Zhang, Yi He
Ping Jiang, Yuan Guo, Yi He, Department Of Cardiology, Zhuzhou Central Hospital, Zhuzhou 412000, Hunan Province, China
Liang Xiao, Department of Pediatric, Zhuzhou Central Hospital, Zhuzhou 412000, Hunan Province, China
Rong Hu, Bo-Yi Zhang, Department of Medical Ultrasonics, Zhuzhou Central Hospital, Zhuzhou 412000, Hunan Province, China
Author contributions: Jiang P and He Y reviewed the literature and contributed to manuscript drafting; Hu R and Zhang YB performed follow-up work and interpreted the data; Xiao L and Guo Y analyzed and interpreted the gene sequencing; all authors approved the final version to be submitted.
Supported by Natural Science Foundation of Hunan Province, No. 2019JJ60087.
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: The authors declare that they have no conflicts of interest.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Yi He, MBBS, Chief Physician, Department Of Cardiology, Zhuzhou Central Hospital, No. 118 South Changjiang Road, Zhuzhou 412000, Hunan Province, China. heyicardiology@163.com
Received: October 5, 2021
Peer-review started: October 5, 2021
First decision: November 11, 2021
Revised: November 21, 2021
Accepted: January 19, 2022
Article in press: January 19, 2022
Published online: March 6, 2022
Core Tip

Core Tip: We present the case of an infant with dilated cardiomyopathy (DCM) who was diagnosed with Alström syndrome at the early stage of the disease. Whole-exome sequencing revealed that a large deletion and point mutation simultaneously occurred in the Alström syndrome 1 (ALMS1) gene, leading to frameshift and missense mutations, respectively, rather than nonsense or frameshift mutations, which have been reported previously. Likewise, to date, few interpretations have been made of the related mechanism of the novel ALMS1 gene mutation to induce DCM in infants.