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Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
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| Published in: | Case Reports in Genetics |
|---|---|
| Format: | Online Article RSS Article |
| Published: |
2025
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| _version_ | 1868552983441047552 |
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| collection | WordPress RSS FRELIP Feed Integration |
| container_title | Case Reports in Genetics |
| description | |
| discipline_display | Genetics |
| discipline_facet | Genetics |
| format | Online Article RSS Article |
| genre | Journal Article |
| id | rss_article:70862 |
| institution | FRELIP |
| journal_source_facet | Case Reports in Genetics |
| last_indexed | 2026-06-20T21:29:44.956Z |
| publishDate | 2025 |
| publishDateSort | 2025 |
| record_format | rss_article |
| spellingShingle | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature Genetics General Genetics |
| sub_discipline_display | General |
| sub_discipline_facet | General |
| subject_display | Genetics General Genetics |
| subject_facet | Genetics General Genetics |
| title | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature |
| title_alt | Presentación rara de mutaciones homocigotas de SLC20A2 que causan vasculopatía cerebral intraarterial y accidente cerebrovascular en la infancia: reporte de caso y revisión de la literatura Présentation rare de mutations homozygotes de SLC20A2 causant une vasculopathie cérébrale intra-artérielle et un accident vasculaire cérébral chez le nourrisson : rapport de cas et revue de la littérature Apresentação Rara de Mutações Homozigóticas SLC20A2 Causando Vasculopatia Cerebral Intra-Arterial e AVC na Infância: Relato de Caso e Revisão da Literatura |
| title_auth | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature |
| title_es_txt | Presentación rara de mutaciones homocigotas de SLC20A2 que causan vasculopatía cerebral intraarterial y accidente cerebrovascular en la infancia: reporte de caso y revisión de la literatura |
| title_fr_txt | Présentation rare de mutations homozygotes de SLC20A2 causant une vasculopathie cérébrale intra-artérielle et un accident vasculaire cérébral chez le nourrisson : rapport de cas et revue de la littérature |
| title_full | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature |
| title_fullStr | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature |
| title_full_unstemmed | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature |
| title_pt_txt | Apresentação Rara de Mutações Homozigóticas SLC20A2 Causando Vasculopatia Cerebral Intra-Arterial e AVC na Infância: Relato de Caso e Revisão da Literatura |
| title_short | Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature |
| title_sort | rare presentation of homozygous slc20a2 mutations causing intra-arterial cerebral vasculopathy and stroke in infancy: case report and review of the literature |
| topic | Genetics General Genetics |
| url | https://www.hindawi.com/journals/crig/2025/1587968/ |