[Von Hippel Lindau disease: about one case]
Revue Maghrebine d'Endocrinologie-Diabete et de Reproduction [La]. 2008; 14 (4): 183-186
em Fr
| IMEMR
| ID: emr-108784
Biblioteca responsável:
EMRO
ABSTRACT
Von Hippel Lindau disease is an autosomal dominant inherited disorder secondary to a mutation of the VHL gene, localisated on the chromosome 3, which is a tumor suppressor gene. Tumoral manifestations include hemangioblastomas, renal cysts and/or tumors, pancreatic cysts and/or neuroendocrine tumors, pheochromocytomas and endolymphatic sac tumors. Early diagnosis is necessary to allow for a regular follow up of the patient and his descendants
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Índice:
IMEMR
Assunto principal:
Feocromocitoma
/
Hemangioblastoma
/
Doença de von Hippel-Lindau
Tipo de estudo:
Case_reports
/
Screening_studies
Limite:
Humans
/
Male
Idioma:
Fr
Revista:
Rev. Maghreb. Endocrinol.-Diabete Reprod.
Ano de publicação:
2008