Familial Von Hippel–Lindau Disease: A Case Series of Cerebral Hemangioblastomas with MRI, Histopathological, and Genetic Correlations

Von Hippel-Lindau (VHL) is a rare genetic disorder caused by mutations in the VHL gene on chromosome 3. The disease is associated with increased incidence of neoplasia. The most common manifestations of the disease are hemangioblastomas of the CNS and spinal cord, followed by renal cell carcinomas (...

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主要な著者:	Claudiu Matei, Ioana Boeras, Dan Orga Dumitriu, Cosmin Mutu, Adriana Popescu, Mihai Gabriel Cucu, Alexandru Calotă-Dobrescu, Bogdan Fetica, Diter Atasie
フォーマット:	Artigo
言語:	Inglês
出版事項:	MDPI AG 2025-10-01
シリーズ:	Life
主題:	Von-Hippel Lindau VHL hemangioblastoma genetic disease
オンライン･アクセス:	https://www.mdpi.com/2075-1729/15/11/1649
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