Von Hippel-Lindau disease is a genetic disorder caused by a mutation on the third chromosome. In healthy individuals, the chromosome has a Von Hippel-Lindau tumor suppressor, while individuals with the disorder are lacking this suppressor.
Von Hippel-Lindau Disease
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Von Hippel-Lindau Disease
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Von Hippel-Lindau disease (VHL) is a rare genetic disorder (affecting approximately 1 in 36,000 people) in which some blood vessels grow in an abnormal way and cause tumors in parts of the body that are rich in blood vessels.
Causes ...
Von-Hippel Lindau disease is caused by a particular gene fault. The VHL gene is a tumour suppressor gene, so it normally stops the overgrowth and division of cells. If the gene is faulty (mutated) it can lead to the development of particular cancers.
von Hippel-Lindau disease
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Micrograph of cerebellar hemangioblastoma. HPS stain.
Von Hippel-Lindau disease (an inherited condition that causes abnormal growth of blood vessels).
Tuberous sclerosis (an inherited disease marked by noncancerous fatty cysts in the kidney).
Von Hippel-Lindau disease.
The most infamous feud in American folklore, the long-running battle between the Hatfields and McCoys, may be partly explained by a rare, inherited disease that can lead to hair-trigger rage and violent outbursts.
Von Hippel-Lindau disease
Angioma proliferation in the retina, brain, spinal cord, and adrenal glands
Autosomal Recessive ...
Von Hippel-Lindau Disease.
By Singh AD, Shields CL, Shields JA
Related Articles von Hippel-Lindau disease. Surv Ophthalmol. 2001 Sep-Oct;46(2):117-… more… ...
von Hippel-Lindau disease: An inherited condition that occurs in 50 percent of children with an affected parent.
Von Hippel-Lindau disease (VHL)
A rare, genetic multisystem disorder characterized by the abnormal growth of tumors in certain parts of the body (angiomatosis).
Lindau Disease
Linear Nevus Sebacous Syndrome
Linear Sebaceous Nevus Sequence
Linear Sebaceous Nevus Syndrome
Lingua Fissurata
Lingua Nigra
Lingua Plicata
Lingua Scrotalis
Lingua Villosa Nigra
Linguofacial Dyskinesia ...
Individuals with tuberous sclerosis, neurofibromatosis (type 1 and 2), familial polyposis, and von Hippel-Lindau disease have a higher incidence of brain tumors.
Neurofibromatosis ...
DRPM, Design, Experimental, Docusate Calcium, Endo-1,4-beta-Glucanase, Enhancements, Genetic, Food Technology, Gait, Duck, Gene Expression Chip, Infantile Hypertonia, Labor Presentations, Lamiaceae, Larynx Neoplasms, Lindau Disease, ...
neurofibromatosis, von Hippel-Lindau disease, Li-Fraumeni syndrome, and retinoblastoma) also have an increased risk to develop tumors of the central nervous system.
renal cell cancer, kidney cancer, paraneoplastic syndromes, renal cancer, von Hippel-Lindau syndrome, VHL syndrome, von Hippel-Lindau disease, VHL disease, renal cell carcinoma, metastasis, cystic kidney disease, chronic renal insufficiency, ...
Angiomas (swelling of the blood vessels) of the retina may occur, usually in association with a syndrome called Von Hippel-Lindau disease (an hereditary disease causing vascular nodules in the retina).
Having certain genetic conditions, such as von Hippel-Lindau disease or hereditary papillary renal cell carcinoma.
Possible signs of renal cell cancer include blood in the urine and a lump in the abdomen.
Family history. Some genetic conditions, such as von Hippel-Lindau disease, Turcot syndrome, or neurofibromatosis, increase the risk of developing a brain tumor. Genetic predisposition accounts for less than 5% of brain tumors.
Neurofibromatosis type 1 or 2
von Hippel-Lindau disease
Tuberous sclerosis
Li-Fraumeni syndrome
Turcot syndrome type 1 and type 2
Klinefelter syndrome
Nevoid basal cell carcinoma syndrome ...
Hepatolenticular Degeneration; Herniated Lumbar Disk; Hippel-Lindau Disease; Hypersensitivity Lung Disease
BR
Brain; Breech; Bregma; Bridge; Bromine; Bronchitis; Brown; Brucella; Brucellosis ...
For example, multiple hemangioblastomas are associated with von Hippel-Lindau disease (VHL), an inherited tumor syndrome.
Children with certain genetic conditions (such as neurofibromatosis, von Hippel-Lindau disease, Li-Frameni syndrome, Gorlin’s syndrome and retinoblastoma) have an increased risk of developing tumors of the central nervous system.
Dialysis treatment
Family history of the disease
Genetics
Smoking
Von Hippel-Lindau disease (a hereditary disease that affects the capillaries of the brain, eyes, and other body parts)
Pictures & Images ...
Angiomatosis retinae
Cerebelloretinal Angiomatosis, Familial
Hippel-Lindau Disease
VHL syndrome
von Hippel-Lindau Disease ...
Von Hippel Lindau disease
Von Hippel-Lindau Syndrome
von Meyenburg Disease
von Mikulicz Syndrome
von Mikulicz's Aphthae
Von Recklinghausen's disease
Von Recklinghausen's neurofibromatosis
Von Willebrand Disease ...
Vincent's disease
vivax malaria
Von Gierke's disease
von hippel-lindau disease
von Recklinghausen's disease
Von Willebrand disease
Von Willebrand's disease ...
Neurofibromatosis
Tuberous sclerosis
Von Hippel-Lindau disease
Li-Fraumeni syndrome
Turcot's syndrome ...
Dialysis treatment
Family history of the disease
Genetics
High blood pressure
Horseshoe kidney
Smoking
Von Hippel-Lindau disease (a hereditary disease that affects the capillaries of the brain, eyes, and other body parts) ...
In many cases, the cause of a particular pancreatic cyst is unknown. Some cysts are associated with rare illnesses — such as von Hippel-Lindau disease, which is a genetic disorder that can affect the brain, retina, adrenal glands, ...
Vascular Erectile Tumor
Vasculitis Syndromes of the Central and Peripheral Nervous Systems
Von Economo's Disease
Von Hippel-Lindau Disease (VHL)
Von Recklinghausen's Disease ...
Smoking.
Obesity.
Hypertension.
Family history of the disease.
Dialysis patients with cysts in their kidneys.
Inherited disorders such as von Hippel-Lindau disease.
Neurofibromatosis type 2 (brain and spinal cord tumors)
Retinoblastoma (malignant retinal glioma, or tumors originating from glial cells)
Tuberous sclerosis (primary brain tumors)
Von Hippel-Lindau disease (retinal tumor, ...
include childhood disease risk such as retinoblastoma, multiple endocrine neoplasia (MEN) types 1 and 2 (MEN1 and MEN2), neurofibromatosis types 1 and 2 (NF1 and NF2), Beckwith-Wiedemann syndrome, Fanconi anemia, FAP, and Von Hippel-Lindau disease ...
aspx"vascular anomalies of different types, involving the skin within the clinical manifestations of phakomatosis or neurocutaneous syndromes. Among them Klippel Trnaunay Weber syndrome, von Hippel Lindau disease, ...
Vitamin A deficiency ... blindness, night blindness, night blindness
Vitreous detachment ... retinal detachment
Volubilis, syndrome du ... retinal detachment
Von Hippel-Lindau Disease ... blindness ...
pressure, exposure to environmental toxins (e.g. asbestos), and exposure to radiation may increase a patient's risk of developing kidney cancer. In addition, patients who are undergoing dialysis or who have a history of von Hippel-Lindau disease or ...
occur equally often in men and women and are somewhat less common among blacks than among other races. The condition can be associated with other conditions, including medullary carcinoma of the thyroid, neurofibromatosis, von Hippel-Lindau disease, ...
There are also many other illnesses that may predispose a patient to metastatic renal cancer such as papillary renal cell carcinoma which is hereditary as well as Von Hippel-Lindau disease.
Von Hippel-Lindau disease
Von Willebrand syndrome see Haemophilia, von Willebrand disease and other Coagulation Defects
VSD see Heart Defects
VTEC 0157 infection see Haemolytic Uraemic syndrome ...
Von Hippel-Lindau Disease (0 images)
Vulva Carcinoma (0 images)
Vulvitis Plasmacellularis (0 images)
Waldenström's Macroglobulinaemia (0 images)
Wasp / Bee Sting (0 images)
Watchglass Nails (5 images)
Waterhouse-Friedrichsen Syndrome (0 images) ...
 See also: Von Hippel-Lindau, Von Hippel-lindau Disease, Cancer, Sclerosis, Melanoma
  
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