Cargando…
A spinal cord compression syndrome revealing neurofibromatosis type 1: A case report
Neurofibromatosis type 1 (NF1), formerly known as von Recklinghausen disease is an autosomal dominant disease with multisystem involvement. In the peripheral nervous system, it leads to the development of benign tumors from the tissue of the spinal or cranial nerve sheaths, known as “neurofibromas.”...
Autores principales: | Traore, Wend-Yam Mohamed, Merbouh, Sahar, Diallo, Ibrahima Dokal, Cherif, Kettani Ech, Jiddane, Mohamed, Touarsa, Firdous |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336349/ https://www.ncbi.nlm.nih.gov/pubmed/37448607 http://dx.doi.org/10.1016/j.radcr.2023.06.032 |
Ejemplares similares
-
Bone Manifestations of Neurofibromatosis Type 1
por: Diallo, Ibrahima Dokal, et al.
Publicado: (2022) -
Lipid‐poor vertebral hemangioma mimicking a vertebral metastasis of cervical carcinoma
por: Traore, Wend‐Yam Mohamed, et al.
Publicado: (2023) -
Brain iron accumulation on MRI revealing aceruloplasminemia: a rare cause of simultaneous brain and systemic iron overload
por: Touarsa, Firdaous, et al.
Publicado: (2022) -
A rare case of Fahr disease revealed by an epileptic seizure
por: Choayb, Safaa, et al.
Publicado: (2023) -
Septo-optic dysplasia PLUS syndrome in a 23 years old patient: A case report
por: Harras, Yahya EL, et al.
Publicado: (2023)