HYPOMELANOSIS OF ITO WITH EPILEPSY: TWO CASES IN CLINICAL PRACTICE
Abstract
Hypomelanosis of Ito (HI) is rare genetic disorder of the phakomatoses group. Authors represent literature review on the history of the HI description, etiology, clinical features, diagnosis, and approaches to therapy. Special attention is description is characteristics of epilepsy and EEG to HI. We also discuss different approaches to the treatment of epilepsy. So HI is rare disease the authors carried out a comparative analysis of the observed two patients with HI and epilepsy with literature data.
About the Authors
M. B. Mironov
Institute of Child Neurology and Epilepsy them. St. Luke, Moscow
Russian Federation
Russian Federation
N. Yu. Borovikova
Institute of Child Neurology and Epilepsy them. St. Luke, Moscow
Russian Federation
Russian Federation
K. S. Borovikov
Institute of Child Neurology and Epilepsy them. St. Luke, Moscow
Russian Federation
Russian Federation
K. Yu. Mukhin
Institute of Child Neurology and Epilepsy them. St. Luke, Moscow
Russian Federation
Russian Federation
References
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Review
For citations:
Mironov M.B., Borovikova N.Yu., Borovikov K.S., Mukhin K.Yu. HYPOMELANOSIS OF ITO WITH EPILEPSY: TWO CASES IN CLINICAL PRACTICE. Epilepsy and paroxysmal conditions. 2012;4(1):8-12. (In Russ.)
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