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

doi:10.22541/au.162675256.68454481/v1

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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

Abstract

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

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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

Jun 2022Published in Clinical Case Reports volume 10 issue 6. 10.1002/ccr3.5958

Abstract

Peer review status:Published