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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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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 |
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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 |
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