A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and
review of the literature
- tian qin deng
, - qingzhi liu,
- jiansheng xie,
- xuemei li,
- bing yao
qingzhi liu
Southern Medical University Clinical Medical College
Author Profilebing yao
Southern Medical University Clinical Medical College
Author ProfileAbstract
Diagnosis of KBGS due to a high risk identified by early Down's syndrome
screening has not been reported in previous studies, and the prominent
KBGS phenotype and absence of specificity on early ultrasound
examination also pose a challenge for genetic diagnosis.13 Jul 2021Submitted to Clinical Case Reports 15 Jul 2021Submission Checks Completed
15 Jul 2021Assigned to Editor
20 Jul 2021Reviewer(s) Assigned
11 Nov 2021Review(s) Completed, Editorial Evaluation Pending
06 Mar 2022Editorial Decision: Revise Minor
28 Mar 20221st Revision Received
01 Apr 2022Submission Checks Completed
01 Apr 2022Assigned to Editor
01 Apr 2022Review(s) Completed, Editorial Evaluation Pending
28 May 2022Editorial Decision: Accept
