Pecold K, Ziemiański A, Bernardczyk-Meller J, Krawczyński M, Sosnowski P
Kliniki Okulistycznej AM w Poznaniu.
Klin Oczna. 1995 Jun;97(6):161-3.
Von Hippel-Lindau disease belongs to phakomatosis. It is a dominantly autosomally inherited disease. The aim of the study was to present and evaluate different methods of diagnostic examinations (computer tomography, magnetic resonance imaging and ultrasonography) in 14 patients with the disease. The results of investigations showed a wide variety of visceral manifestations. All the patients are carefully followed up. Control examinations every six months allow to check for and treat any new pathological changes in the retina.
冯·希佩尔-林道病属于 phakomatosis。它是一种常染色体显性遗传病。本研究的目的是介绍并评估14例患有该疾病的患者的不同诊断检查方法（计算机断层扫描、磁共振成像和超声检查）。调查结果显示出多种内脏表现。所有患者都得到了密切随访。每六个月进行一次对照检查，以便检查并治疗视网膜中的任何新的病理变化。
