Lindau disease

von Hip·pel-Lin·dau syn·drome

(făn hip'el lan'dow), [MIM*193300]
a type of phacomatosis, consisting of retinal vascular malformations, which may be multiple and bilateral, associated with hemangioblastomas primarily of the cerebellum and walls of the fourth ventricle, occasionally involving the spinal cord; sometimes associated with renal cell carcinomas or cysts or hamartomas of kidney, adrenal, or other organs; autosomal dominant inheritance due to mutation in the von Hippel-Lindau gene (VHL) on 3p.

von Hip·pel-Lin·dau syn·drome

(făn hip'el lan'dow), [MIM*193300]
a type of phacomatosis, consisting of retinal vascular malformations, which may be multiple and bilateral, associated with hemangioblastomas primarily of the cerebellum and walls of the fourth ventricle, occasionally involving the spinal cord; sometimes associated with renal cell carcinomas or cysts or hamartomas of kidney, adrenal, or other organs; autosomal dominant inheritance due to mutation in the von Hippel-Lindau gene (VHL) on 3p.

Lindau disease

(lin'dow?)
[Arvid Lindau, Swedish pathologist, 1892–1958]
Lindau–von Hippel disease.

Lindau,

Arvid Wilhelm, Swedish pathologist, 1892-1958.
Lindau disease - Synonym(s): von Hippel-Lindau syndrome
Lindau tumor - a benign cerebellar neoplasm. Synonym(s): hemangioblastoma
von Hippel-Lindau syndrome - see under von Hippel
References in periodicals archive ?
Differential diagnosis: Polycystic liver disease, tuberous sclerosis, autosomal recessive polycystic disease (ARPD), Von Hippel Lindau disease, and multiple simple cysts in the liver and kidneys.