loading page

A Rare Case of 2q37 Deletion Syndrome Presented with Patent Foramen Ovale
  • +2
  • Ahmed Zaki,
  • Nour Shaheen,
  • Abdelraouf Ramadan,
  • Abdelraouf Ramadan,
  • Abdulqadir Nashwan
Ahmed Zaki
Cairo University

Corresponding Author:[email protected]

Author Profile
Nour Shaheen
Alexandria University Faculty of Medicine
Author Profile
Abdelraouf Ramadan
Helwan University
Author Profile
Abdelraouf Ramadan
University of Louisville
Author Profile
Abdulqadir Nashwan
Hamad Medical Corporation
Author Profile


Here we report a patient with 2q37 deletion syndrome confirmed by comparative genomic hybridization (CGH) plus single nucleotide polymorphism (SNP), who does not suffer from mental developmental abnormalities. The patient, however, does suffer from fatigue and gross motor delay, and the presence of a patent foramen ovale.
08 Oct 2022Submitted to Clinical Case Reports
10 Oct 2022Submission Checks Completed
10 Oct 2022Assigned to Editor
19 Oct 2022Reviewer(s) Assigned
07 Dec 2022Review(s) Completed, Editorial Evaluation Pending
09 Dec 2022Editorial Decision: Revise Minor
20 Jan 20231st Revision Received
30 Jan 2023Submission Checks Completed
30 Jan 2023Assigned to Editor
30 Jan 2023Review(s) Completed, Editorial Evaluation Pending
06 Feb 2023Editorial Decision: Accept