Cargando…

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

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 identifyi...

Descripción completa

Detalles Bibliográficos
Autores principales: Zaki, Ahmed, Shaheen, Nour, Hosny, Mohamed, Ramadan, Abdelraouf, Nashwan, Abdulqadir J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658514/
https://www.ncbi.nlm.nih.gov/pubmed/38028106
http://dx.doi.org/10.1002/ccr3.6970
_version_ 1785148226394914816
author Zaki, Ahmed
Shaheen, Nour
Hosny, Mohamed
Ramadan, Abdelraouf
Nashwan, Abdulqadir J.
author_facet Zaki, Ahmed
Shaheen, Nour
Hosny, Mohamed
Ramadan, Abdelraouf
Nashwan, Abdulqadir J.
author_sort Zaki, Ahmed
collection PubMed
description 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.
format Online
Article
Text
id pubmed-10658514
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-106585142023-11-19 A rare case of 2q37 deletion syndrome presented with patent foramen ovale Zaki, Ahmed Shaheen, Nour Hosny, Mohamed Ramadan, Abdelraouf Nashwan, Abdulqadir J. Clin Case Rep Case Report 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. John Wiley and Sons Inc. 2023-11-19 /pmc/articles/PMC10658514/ /pubmed/38028106 http://dx.doi.org/10.1002/ccr3.6970 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Zaki, Ahmed
Shaheen, Nour
Hosny, Mohamed
Ramadan, Abdelraouf
Nashwan, Abdulqadir J.
A rare case of 2q37 deletion syndrome presented with patent foramen ovale
title A rare case of 2q37 deletion syndrome presented with patent foramen ovale
title_full A rare case of 2q37 deletion syndrome presented with patent foramen ovale
title_fullStr A rare case of 2q37 deletion syndrome presented with patent foramen ovale
title_full_unstemmed A rare case of 2q37 deletion syndrome presented with patent foramen ovale
title_short A rare case of 2q37 deletion syndrome presented with patent foramen ovale
title_sort rare case of 2q37 deletion syndrome presented with patent foramen ovale
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658514/
https://www.ncbi.nlm.nih.gov/pubmed/38028106
http://dx.doi.org/10.1002/ccr3.6970
work_keys_str_mv AT zakiahmed ararecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT shaheennour ararecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT hosnymohamed ararecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT ramadanabdelraouf ararecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT nashwanabdulqadirj ararecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT zakiahmed rarecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT shaheennour rarecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT hosnymohamed rarecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT ramadanabdelraouf rarecaseof2q37deletionsyndromepresentedwithpatentforamenovale
AT nashwanabdulqadirj rarecaseof2q37deletionsyndromepresentedwithpatentforamenovale