Fluorodeoxyglucose positron emission tomography-computed tomography scan in von Hippel-Lindau syndrome: A case report and review of literature

Von Hippel-Lindau (VHL) syndrome is a hereditary autosomal dominant disorder caused by defective tumor suppression gene at 3p25-p26. The gene for VHL disease is found on chromosome 3, and is inherited in a dominant fashion. The VHL gene is a tumor suppressor gene. This means that its role in a norma...

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Veröffentlicht in:	Indian journal of nuclear medicine 2012-04, Vol.27 (2), p.119-121
Hauptverfasser:	Solav, Shrikant, Bhandari, Ritu
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report Case studies CT imaging Eye diseases Nuclear medicine PET imaging Tomography Tumors
Online-Zugang:	Volltext
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