Article

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

2022-10-10

Abstract excerpt

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.

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Literature Corpus work: d8d7a05b-5364-559b-ab74-db2b4565fbbd
DOI: 10.22541/au.166540048.86392906/v1

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