Publication Name	World Journal of Clinical Cases
Manuscript ID	57120
Country	China

Category	Gastroenterology & Hepatology
Manuscript Type	Case Report
Article Title	Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature
Manuscript Source	Unsolicited Manuscript
All Author List	Li-Jing Xiong, Mao-Ling Jiang, Li-Na Du, Lan Yuan and Xiao-Li Xie
Funding Agency and Grant Number
Corresponding Author	Li-Jing Xiong, MD, Attending Doctor, Gastroenterology, Hepatology and Nutrition, Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, No. 1617 Riyue Avenue, Chengdu 610091, Sichuan, China. xionglijing1985@qq.com
Key Words	Fanconi–Bickel syndrome; Glucose transporter protein 2; Case report; Children; Chinese;
Core Tip	FBS is a rare genetic metabolic disease causing impaired glucose liver homeostasis and proximal renal tubular dysfunction. Results of urine and blood testing suggesting abnormal glucose metabolism could be the clues for FBS in neonates and infants. Genetic sequencing is indispensable for diagnosis. Since the diversity of disease severity, early identification and long-term follow-up could help improve patients’ quality of life and decrease mortality.
Citation	Xiong LJ, Jiang ML, Du LN, Yuan L, Xie XL. Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literature. World J Clin Cases 2020; 8(21): 5467-5473

Received	2020-05-26 07:01
Peer-Review Started	2020-05-26 07:02
To Make the First Decision
Return for Revision	2020-09-14 01:08
Revised	2020-09-16 13:35
Second Decision	2020-09-25 06:44
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-09-25 22:25
Articles in Press	2020-09-25 22:25
Publication Fee Transferred
Edit the Manuscript by Language Editor	2020-10-07 13:00
Typeset the Manuscript	2020-11-03 00:44

ISSN	2307-8960 (online)
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