LATEST DIAGNOSIS OF NEUROPHYBROMATOSIS I TYPE IN 14-YEAR-OLD BOY

LATEST DIAGNOSIS OF NEUROPHYBROMATOSIS I TYPE IN 14-YEAR-OLD BOY

The article presents modern views on the problem of hereditary progressive pathology: phakomatosis, including neurofibromatosis as the most common in the population of the neurocutaneous syndrome. The main clinical manifestations, diagnostic criteria for neurofibromatosis type I, are considered. Pr...

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Bibliographic Details
Main Authors:	D. I. Sadykova, L. Z. Safina, R. A. Kadyrmetov
Format:	Article
Language:	Russian
Published:	Ltd. “The National Academy of Pediatric Science and Innovation” 2017-09-01
Series:	Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:	children phakomatosis neurofibromatosis i type mental retardation spots "coffee with milk" magnetic resonance imaging
Online Access:	https://www.ped-perinatology.ru/jour/article/view/531

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