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[Preclinical diagnostics of von Hippel-Lindau syndrome in a child]. [PDF]
Probl Endokrinol (Mosk)Malievskiy OA +3 more
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Revealing a Heterozygous <i>FCGR1A</i> Variant in a Patient with Uveal Melanoma and Von Hippel-Lindau Syndrome: A Rare Case Report. [PDF]
J Curr OphthalmolAzimi F +5 more
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CT-derived radiomics predict the growth rate of renal tumours in von Hippel-Lindau syndrome. [PDF]
Clin RadiolSingh S +8 more
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Ophthalmological Aspects of von-Hippel–Lindau Syndrome
Seminars in Ophthalmology, 2021 Background: von Hippel-Lindau (VHL) syndrome is a multisystem neoplastic disorder involving eyes, central nervous system, kidneys, spine, and other tissues. A retinal capillary hemangioma (RCH) is the earliest manifestation of the VHL disease in most cases.Areas covered:This paper aims to provide an up-to-date review of the current literature about von
Hashim Ali Khan +10 more
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Cancer, 1999
Von Hippel-Lindau (VHL) syndrome (OMIM 193300) is an autosomal dominant disorder caused by deletions or mutations in a tumor suppressor gene mapped to human chromosome 3p25. It is characterized clinically by vascular tumors, including retinal and central nervous system hemangioblastomas (cerebellar, spinal, and brain stem). Hemangioblastomas are benign
exaly +4 more sources
Von Hippel-Lindau (VHL) syndrome (OMIM 193300) is an autosomal dominant disorder caused by deletions or mutations in a tumor suppressor gene mapped to human chromosome 3p25. It is characterized clinically by vascular tumors, including retinal and central nervous system hemangioblastomas (cerebellar, spinal, and brain stem). Hemangioblastomas are benign
exaly +4 more sources
Pancreatic Lesions in the Von Hippel-Lindau Syndrome.
Gastroenterology, 1991Common manifestations of the von Hippel-Lindau syndrome, an autosomally dominant inherited cancer-prone disorder, include retinal angiomatosis, hemangioblastoma of the central nervous system, renal cysts, renal cancer, pheochromocytoma, and epididymal cystadenoma.
Hartmut P H Neumann +2 more
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Der Radiologe, 2013
Von Hippel-Lindau syndrome is an autosomal dominant inherited phacomatosis with a predisposition for the central nervous system and retina. There is variable expression with hemangioblastomas in the brain, medulla oblongata, spinal chord, renal carcinoma, pheochromocytoma, pancreatic cysts and islet cell tumors as well as tumors of the endolymphatic ...
W, Reith, H, Körner
openaire +2 more sources
Von Hippel-Lindau syndrome is an autosomal dominant inherited phacomatosis with a predisposition for the central nervous system and retina. There is variable expression with hemangioblastomas in the brain, medulla oblongata, spinal chord, renal carcinoma, pheochromocytoma, pancreatic cysts and islet cell tumors as well as tumors of the endolymphatic ...
W, Reith, H, Körner
openaire +2 more sources