A Rare Case of 2q37 Deletion Syndrome Presented with Patent Foramen Ovale

Ahmed  Zaki; Nour  Shaheen; Abdelraouf  Ramadan; Abdelraouf  Ramadan; Abdulqadir Nashwan

doi:10.22541/au.166540048.86392906/v1

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A Rare Case of 2q37 Deletion Syndrome Presented with Patent Foramen Ovale

Ahmed Zaki,
Nour Shaheen,
Abdelraouf Ramadan,
Abdelraouf Ramadan,
Abdulqadir Nashwan

Abstract

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

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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

Abstract

Peer review status:ACCEPTED