A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case
The neurological disorder known as Dyke-Davidoff-Masson syndrome (DDMS) was initially identified in 1933 as hemispheric atrophy. Clinical signs and symptoms include mental impairment, seizures, facial asymmetry, and contralateral hemiparesis. Asymmetric thickening of the calvarium and expansion of t...
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| Format: | Article |
| Language: | English |
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Wolters Kluwer – Medknow Publications
2024-12-01
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| Series: | Journal of Integrated Health Sciences |
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| Online Access: | https://journals.lww.com/10.4103/jihs.jihs_22_24 |
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| author | Akash Shah Meetkumar Patel Shubham Darda Sweta Sanandia |
| author_facet | Akash Shah Meetkumar Patel Shubham Darda Sweta Sanandia |
| author_sort | Akash Shah |
| collection | DOAJ |
| description | The neurological disorder known as Dyke-Davidoff-Masson syndrome (DDMS) was initially identified in 1933 as hemispheric atrophy. Clinical signs and symptoms include mental impairment, seizures, facial asymmetry, and contralateral hemiparesis. Asymmetric thickening of the calvarium and expansion of the frontal and ethmoid sinuses are among the neuroimaging findings. We present here a case of 19-year-old male who is known case of epilepsy with complaints of multiple episodes of seizures frequently and on magnetic resonance imaging was diagnosed to have DDMS. |
| format | Article |
| id | doaj-art-7fb4c8a3d1a3458fadac8bfbcae6c6e4 |
| institution | Kabale University |
| issn | 2347-6486 2347-6494 |
| language | English |
| publishDate | 2024-12-01 |
| publisher | Wolters Kluwer – Medknow Publications |
| record_format | Article |
| series | Journal of Integrated Health Sciences |
| spelling | doaj-art-7fb4c8a3d1a3458fadac8bfbcae6c6e42025-08-20T03:44:10ZengWolters Kluwer – Medknow PublicationsJournal of Integrated Health Sciences2347-64862347-64942024-12-0112217317510.4103/jihs.jihs_22_24A Case Report of a Rare Dyke-Davidoff-Masson Syndrome CaseAkash ShahMeetkumar PatelShubham DardaSweta SanandiaThe neurological disorder known as Dyke-Davidoff-Masson syndrome (DDMS) was initially identified in 1933 as hemispheric atrophy. Clinical signs and symptoms include mental impairment, seizures, facial asymmetry, and contralateral hemiparesis. Asymmetric thickening of the calvarium and expansion of the frontal and ethmoid sinuses are among the neuroimaging findings. We present here a case of 19-year-old male who is known case of epilepsy with complaints of multiple episodes of seizures frequently and on magnetic resonance imaging was diagnosed to have DDMS.https://journals.lww.com/10.4103/jihs.jihs_22_24dyke-davidoff-masson syndromehemiparesisseizure |
| spellingShingle | Akash Shah Meetkumar Patel Shubham Darda Sweta Sanandia A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case Journal of Integrated Health Sciences dyke-davidoff-masson syndrome hemiparesis seizure |
| title | A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case |
| title_full | A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case |
| title_fullStr | A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case |
| title_full_unstemmed | A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case |
| title_short | A Case Report of a Rare Dyke-Davidoff-Masson Syndrome Case |
| title_sort | case report of a rare dyke davidoff masson syndrome case |
| topic | dyke-davidoff-masson syndrome hemiparesis seizure |
| url | https://journals.lww.com/10.4103/jihs.jihs_22_24 |
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