NEUROFIBROMATOSIS - CLINICAL POLYMORPHISM AND TREATMENT APPROACHES
- Authors: 1, 1, Lubchenko L.N.2, Filippova M.G.2
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Affiliations:
- НИИ клинической онкологии РОНЦ им. Н.Н. Блохина РАМН
- N.N. Blokhin Russian Cancer Research Center
- Issue: Vol 3, No 4 (2011)
- Pages: 29-36
- Section: Articles
- Published: 11.11.2011
- URL: https://sarbon.abvpress.ru/jour/article/view/252
- ID: 252
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Abstract
Neurofibromatosis consists of several genetically separate diseases - neurofibromatosis type I, neurofibromatosis type II, shwannomatosis and several clinical syndromes of unknown origin. This review discusses diagnostic criteria of neurofibromatosis type I, neurofibromatosis type II, shwannomatosis, novel data on molecular-genetic characteristics, phenotype-genotype correlations, mechanisms of pathogenesis and treatment approaches.
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About the authors
НИИ клинической онкологии РОНЦ им. Н.Н. Блохина РАМН
Author for correspondence.
Email: clingen@mail.ru
Russian Federation
НИИ клинической онкологии РОНЦ им. Н.Н. Блохина РАМН
Russian Federation
L. N. Lubchenko
N.N. Blokhin Russian Cancer Research CenterRussian Federation
M. G. Filippova
N.N. Blokhin Russian Cancer Research CenterRussian Federation
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