A rare case of 2q37 deletion syndrome presented with patent foramen ovale
<div><p>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...
محفوظ في:
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| مؤلفون آخرون: | , , , |
| منشور في: |
2023
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إضافة وسم
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| _version_ | 1864513532434841600 |
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| author | Ahmed Zaki (2127649) |
| author2 | Nour Shaheen (14034758) Mohamed Hosny (7036292) Abdelraouf Ramadan (17687433) Abdulqadir J. Nashwan (11659453) |
| author2_role | author author author author |
| author_facet | Ahmed Zaki (2127649) Nour Shaheen (14034758) Mohamed Hosny (7036292) Abdelraouf Ramadan (17687433) Abdulqadir J. Nashwan (11659453) |
| author_role | author |
| dc.creator.none.fl_str_mv | Ahmed Zaki (2127649) Nour Shaheen (14034758) Mohamed Hosny (7036292) Abdelraouf Ramadan (17687433) Abdulqadir J. Nashwan (11659453) |
| dc.date.none.fl_str_mv | 2023-11-19T03:00:00Z |
| dc.identifier.none.fl_str_mv | 10.1002/ccr3.6970 |
| dc.relation.none.fl_str_mv | https://figshare.com/articles/journal_contribution/A_rare_case_of_2q37_deletion_syndrome_presented_with_patent_foramen_ovale/24954645 |
| dc.rights.none.fl_str_mv | CC BY 4.0 info:eu-repo/semantics/openAccess |
| dc.subject.none.fl_str_mv | Biomedical and clinical sciences Cardiovascular medicine and haematology 2q37 deletion syndrome cardiac anomalies chromosome 2 comparative genomic hybridization patent foramen ovale single nucleotide polymorphism |
| dc.title.none.fl_str_mv | A rare case of 2q37 deletion syndrome presented with patent foramen ovale |
| dc.type.none.fl_str_mv | Text Journal contribution info:eu-repo/semantics/publishedVersion text contribution to journal |
| description | <div><p>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.</p><p> </p></div><h2>Other Information</h2> <p> Published in: Clinical Case Reports<br> License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1002/ccr3.6970" target="_blank">https://dx.doi.org/10.1002/ccr3.6970</a></p> |
| eu_rights_str_mv | openAccess |
| id | Manara2_7dabffe1088dbae36f87a26c22c324ed |
| identifier_str_mv | 10.1002/ccr3.6970 |
| network_acronym_str | Manara2 |
| network_name_str | Manara2 |
| oai_identifier_str | oai:figshare.com:article/24954645 |
| publishDate | 2023 |
| repository.mail.fl_str_mv | |
| repository.name.fl_str_mv | |
| repository_id_str | |
| rights_invalid_str_mv | CC BY 4.0 |
| spelling | A rare case of 2q37 deletion syndrome presented with patent foramen ovaleAhmed Zaki (2127649)Nour Shaheen (14034758)Mohamed Hosny (7036292)Abdelraouf Ramadan (17687433)Abdulqadir J. Nashwan (11659453)Biomedical and clinical sciencesCardiovascular medicine and haematology2q37 deletion syndromecardiac anomalieschromosome 2comparative genomic hybridizationpatent foramen ovalesingle nucleotide polymorphism<div><p>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.</p><p> </p></div><h2>Other Information</h2> <p> Published in: Clinical Case Reports<br> License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1002/ccr3.6970" target="_blank">https://dx.doi.org/10.1002/ccr3.6970</a></p>2023-11-19T03:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.1002/ccr3.6970https://figshare.com/articles/journal_contribution/A_rare_case_of_2q37_deletion_syndrome_presented_with_patent_foramen_ovale/24954645CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/249546452023-11-19T03:00:00Z |
| spellingShingle | A rare case of 2q37 deletion syndrome presented with patent foramen ovale Ahmed Zaki (2127649) Biomedical and clinical sciences Cardiovascular medicine and haematology 2q37 deletion syndrome cardiac anomalies chromosome 2 comparative genomic hybridization patent foramen ovale single nucleotide polymorphism |
| status_str | publishedVersion |
| 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 | A rare case of 2q37 deletion syndrome presented with patent foramen ovale |
| topic | Biomedical and clinical sciences Cardiovascular medicine and haematology 2q37 deletion syndrome cardiac anomalies chromosome 2 comparative genomic hybridization patent foramen ovale single nucleotide polymorphism |