Guidelines for the Multidisciplinary Diagnosis and Treatment of Neurofibromatosis Type 1(2023 Version)

Guidelines for the Multidisciplinary Diagnosis and Treatment of Neurofibromatosis Type 1(2023 Version)

Neurofibromatosis type 1(NF1) is an autosomal dominant hereditary neoplastic disease caused by mutations in the NF1 gene. Features of disorder typically appear in early childhood. The clinical phenotypes of the patients are diverse but neurofibromas is the main feature. Patients with NF1 also suffer...

Olles dieđut

Bibliográfalaš dieđut
Váldodahkki: Multidisciplinary Diagnosis and Treatment Collaboration Group for Neurofibromatosis Type 1 of China Alliance for Rare Diseases
Materiálatiipa: Artihkal
Giella:zho
Almmustuhtton: Editorial Office of Journal of Rare Diseases 2023-04-01
Ráidu:罕见病研究
Fáttát:
neurofibromatosis type 1
multi-discipline
guideline
Liŋkkat:https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2023.02.009

Interneahtta

https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2023.02.009

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