The gene diagnosis of neurofibromatosis type I with headache as the main symptom: A case report and review of the literature
Neurofibromatosis type I (NF1) is an autosomal dominant disease. Some NF1 patients experience atypical clinical manifestations, genetic testing is not widely available, and the types of mutations vary; thus, they are prone to misdiagnosis and missed diagnosis. Although headache is not included in th...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2022-08-01
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| Col·lecció: | Frontiers in Neurology |
| Matèries: | |
| Accés en línia: | https://www.frontiersin.org/articles/10.3389/fneur.2022.874613/full |
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