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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376313/ https://www.ncbi.nlm.nih.gov/pubmed/35979058 http://dx.doi.org/10.3389/fneur.2022.874613 |