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Hippel-Lindau disease: Difference between revisions
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{{disease|Q85.8|Hippel-Lindau Syndrome}} | {{disease|Q85.8|Hippel-Lindau Syndrome}} | ||
H L syndrome | H L syndrome | ||
also known as Hippel-Lindau disease, occasionally also called retino-cerebellar angiomatosis, is a rare, hereditary tumor disease from the group of so-called phakomatoses. | also known as Hippel-Lindau disease, occasionally also called retino-cerebellar angiomatosis, is a rare, hereditary tumor disease from the group of so-called phakomatoses. Patients develop benign, tumor-like tissue changes (angiomas) primarily in the area of the retina of the eye and the cerebellum. The latter has also been referred to as Lindau tumor or Lindau syndrome.<ref>https://de.wikipedia.org/w/index.php?title=Morbus_Hippel-Lindau&oldid=207247719</ref> | ||
[[Category:Medicine]] | |||
Revision as of 00:01, 14 August 2021
Disease classification WHO
Q85.8 Hippel-Lindau Syndrome
H L syndrome also known as Hippel-Lindau disease, occasionally also called retino-cerebellar angiomatosis, is a rare, hereditary tumor disease from the group of so-called phakomatoses. Patients develop benign, tumor-like tissue changes (angiomas) primarily in the area of the retina of the eye and the cerebellum. The latter has also been referred to as Lindau tumor or Lindau syndrome.[1]