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...
Na minha lista:
| Principais autores: | , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Frontiers Media S.A.
2022-08-01
|
| Serier: | Frontiers in Neurology |
| Fag: | |
| Online adgang: | https://www.frontiersin.org/articles/10.3389/fneur.2022.874613/full |
| Tags: |
Ingen Tags, Vær først til at tagge denne postø!
|