TY  - JOUR
AU  - Julia Brasileiro de Faria Cavalcante
AU  - Pedro Nogarotto Cembraneli
AU  - Italo Nogarotto Cembraneli
AU  - Renata Brasileiro de Faria Cavalcante
AU  - José Edison da Silva Cavalcante
AU  - Leonardo Taveira Lopes
AU  - Alessandro Fonseca Cardoso
AU  - Chrystiano Fonseca Cardoso
PY  - 2025
DA  - 2025/02/20
TI  - Cerebellar Hemangioblastoma in A Patient With Von Hippel-Lindau Syndrome
JO  - Neurology and Neuroscience
VL  - 6
IS  - 2
AB  - Von Hippel-Lindau syndrome (VHL) is an autosomal dominant hereditary disease characterized by
a variety of benign/malignant tumors, mainly hemangioblastomas, renal, pancreatic, and hepatic
alterations, as well as pheochromocytoma. The disease is associated with high morbidity and mortality
and can affect multiple family members. Due to the potential for serious complications and psychosocial
impacts, early diagnosis is crucial for monitoring tumor lesions, multidisciplinary treatment, and
appropriate genetic counseling.
SN  - 2692-7918
UR  - https://dx.doi.org/10.33425/2692-7918.1081
DO  - 10.33425/2692-7918.1081