A Rare Co-Occurrence of Maffucci Syndrome and Astrocytoma with IDH1 R132H Mutation: A Case Report

Background: Maffucci syndrome is a rare genetic disorder associated with the development of multiple enchondromas and soft tissue cavernous hemangiomas, as well as an increased risk of malignant tumors. Case Description: Here we report a case of Maffucci syndrome in a patient who presented with a gi...

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Detalles Bibliográficos
Autores principales: Ashirov, Nurali, Mammadinova, Iroda, Moldabekov, Aidos, Zhetpisbaev, Berik, Teltayev, Daniyar, Ryskeldiyev, Nurzhan, Akshulakov, Serik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302001/
https://www.ncbi.nlm.nih.gov/pubmed/37374260
http://dx.doi.org/10.3390/medicina59061056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302001/
https://www.ncbi.nlm.nih.gov/pubmed/37374260
http://dx.doi.org/10.3390/medicina59061056

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