Von Hippel–Lindau Syndrome: A Case Report
BACKGROUND AND OBJECTIVE: Von Hippel–lindau syndrome is a rare syndrome. Von Hippel–Lindau is an autosomal dominant condition manifested by cerebellar and spinal hemangioblastomas, retinal angiomas, clear cell RCC, cysts of the pancreas, kidney, and epididymis, epididymal cystadenimas, pheochromocyt...
Guardado en:
| Autores principales: | , , , , , |
|---|---|
| Formato: | article |
| Lenguaje: | EN FA |
| Publicado: |
Babol University of Medical Sciences
2009
|
| Materias: | |
| Acceso en línea: | https://doaj.org/article/091439b5dc674bfba9b855d27c7bdbce |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|