A case report of mesenteric involvement in neurofibromatosis type 1

Mutations in the Neurofibromatosis Type 1 (NF-1) gene, which is located on chromosome 17q11.2, are the cause of NF-1, an autosomal dominant hereditary condition in which tumors of the nerve system develop. Neurological, skeletal, and cutaneous abnormalities are symptoms of the condition. Of all gast...

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Detalles Bibliográficos
Autores principales: Sang, Nguyen Van, Ninh, Tran Phan, Thanh, Dang Trung, Thinh, Nguyen Cuong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479501/
https://www.ncbi.nlm.nih.gov/pubmed/36128353
http://dx.doi.org/10.25259/JCIS_49_2022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479501/
https://www.ncbi.nlm.nih.gov/pubmed/36128353
http://dx.doi.org/10.25259/JCIS_49_2022

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