Prenatal diagnosis of Pfeiffer syndrome type 2 with increased nuchal translucency

Zhi-yang Hu; Sheng Mou Lin; Meng-jie  Zhu; Cindy Ka-Yee  CHEUNG; Tao  Liu; Jin  Zhu

doi:10.22541/au.161953506.64936732/v1

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Prenatal diagnosis of Pfeiffer syndrome type 2 with increased nuchal translucency

Zhi-yang Hu,
Sheng Mou Lin,
Meng-jie Zhu,
Cindy Ka-Yee CHEUNG,
Tao Liu,
Jin Zhu

Abstract

Pfeiffer syndrome (PS) is a rare autosomal dominant genetic disorder characterized by craniosynostosis, broad thumbs / toes. Here we report a case of PS type 2 with increased nuchal translucency at early trimester.

11 Apr 2021Submitted to Clinical Case Reports

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12 Apr 2021Submission Checks Completed

12 Apr 2021Assigned to Editor

27 Apr 2021Reviewer(s) Assigned

01 Jun 2021Review(s) Completed, Editorial Evaluation Pending

16 Jun 2021Editorial Decision: Revise Minor

20 Jul 20211st Revision Received

20 Jul 2021Submission Checks Completed

20 Jul 2021Assigned to Editor

20 Jul 2021Review(s) Completed, Editorial Evaluation Pending

01 Aug 2021Editorial Decision: Revise Minor

23 Sep 20212nd Revision Received

24 Sep 2021Submission Checks Completed

24 Sep 2021Assigned to Editor

24 Sep 2021Review(s) Completed, Editorial Evaluation Pending

11 Oct 2021Editorial Decision: Accept

Oct 2021Published in Clinical Case Reports volume 9 issue 10. 10.1002/ccr3.5001

Abstract

Peer review status:Published