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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...
Autores principales: | Ashirov, Nurali, Mammadinova, Iroda, Moldabekov, Aidos, Zhetpisbaev, Berik, Teltayev, Daniyar, Ryskeldiyev, Nurzhan, Akshulakov, Serik |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
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 |
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