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

<i>Background</i>: 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. <i>Case Description</i>: Here we report a case of Maffucci syndrome in a patient who prese...

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Hlavní autoři: Nurali Ashirov, Iroda Mammadinova, Aidos Moldabekov, Berik Zhetpisbaev, Daniyar Teltayev, Nurzhan Ryskeldiyev, Serik Akshulakov
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI AG 2023-05-01
Edice:Medicina
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On-line přístup:https://www.mdpi.com/1648-9144/59/6/1056
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