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A rare case of 2q37 deletion syndrome presented with patent foramen ovale.

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Bibliographic Details
Title:	A rare case of 2q37 deletion syndrome presented with patent foramen ovale.
Authors:	Zaki, Ahmed, Shaheen, Nour, Hosny, Mohamed, Ramadan, Abdelraouf, Nashwan, Abdulqadir J.
Source:	Clinical Case Reports; Nov2023, Vol. 11 Issue 11, p1-4, 4p
Subject Terms:	PATENT foramen ovale, COMPARATIVE genomic hybridization, DIAGNOSTIC examinations, DEVELOPMENTAL delay, SINGLE nucleotide polymorphisms
Abstract:	This case report presents a 3‐year‐old female child diagnosed with 2q37 deletion syndrome and patent foramen ovale, and the improvement in hypotonia and gross motor delay after 1 year of physical therapy. This case highlights the importance of thorough examination and diagnostic testing in identifying underlying causes of developmental delays. [ABSTRACT FROM AUTHOR]
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Database:	Complementary Index

Description
Abstract:	This case report presents a 3‐year‐old female child diagnosed with 2q37 deletion syndrome and patent foramen ovale, and the improvement in hypotonia and gross motor delay after 1 year of physical therapy. This case highlights the importance of thorough examination and diagnostic testing in identifying underlying causes of developmental delays. [ABSTRACT FROM AUTHOR]
ISSN:	20500904
DOI:	10.1002/ccr3.6970