Cerebral aneurysm associated with Recklinghausen neurofibromatosis: a case study

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Abstract

Recklinghausen neurofibromatosis is a hereditary disease from the group of phakomatoses, which is transmitted in an autosomal dominant manner with high penetrance and manifests itself as multiple pigmented spots on the skin, pigmented moles, tumors of the skin and nerve trunks.

About the authors

R. A. Yakupov

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Email: info@eco-vector.com
Russian Federation

References

  1. Zhao J.Z., Han X.D. Cerebral aneurysm associated with von Recklinghausen’s neurofibromatosis: a case report. // Surg. Neurol. — 1998. — Vol. 50. — P. 592-596

Copyright (c) 1999 Yakupov R.A.

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