The Two Familial Occurence of von Hippel-Lindau Disease Mitsusuke Miyagami 1 , Atsushi Miyagi 1 , Goroh Kido 1 , Kohten Satoh 1 , Takashi Tsubokawa 1 1Department of Neurological Surgery, School of Medicine Nihon University Keyword: von Hippel-Lindau disease , hemangioblastoma , familial occurence pp.683-689
Published Date 1994/7/1
DOI https://doi.org/10.11477/mf.1406900664
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Five cases of von Hippel-Lindau disease in two families were reported. In one family there were 2 cases in a mother (55 years old) and her daughter (26 years old) which had multiple hemangioblas. tomas in the optic nerve, cerebellum and spinal cord in each case. Retinal angioma appeared in the case of daughter, but not in the mother. In the other family there were 3 cases in a father (28 years old), his son (11 years old) and daughter (14 years old). All of them had retinal angioma and cerebellar hemangioblastoma.

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