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Transformation sarcomateuse de la maladie de Recklinghausen

Neurofibromatosis type I is a common genetic disease. Affected patients are 4 times more likely to develop a tumor. Most tumors are benign (neurofibromas). Although these rarely result in malignant tumors, they represent the leading cause of death in patients, thus making neurofibromatosis type I a...

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Bibliografski detalji
Izdano u:Pan Afr Med J
Glavni autori: Barbach, Younes, Mernissi, Fatima Zahra
Format: Artigo
Jezik:Inglês
Izdano: The African Field Epidemiology Network 2021
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8164437/
https://ncbi.nlm.nih.gov/pubmed/34104304
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2021.38.256.16742
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