MRT peculiarities of posterior cranial fossa in family syringomyelia

A. V. Selezneva , E. G. Mendelevich , I. M. Mikhailov , L. R. Valieva , E. I. Bogdanov

Neurology Bulletin ›› 2003, Vol. XXXV ›› Issue (1-2) : 44 -46.

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Neurology Bulletin ›› 2003, Vol. XXXV ›› Issue (1-2) :44 -46. DOI: 10.17816/nb89666
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MRT peculiarities of posterior cranial fossa in family syringomyelia

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Abstract

It was found that syringomyelic patients and clinically healthy people out of the families with MRT-features of Chiari malformation, type I, had a confident decrease of depth and square of posterior cranial fossa. Relatives of patients, having no signs of Chiari malformation, type I, had the same changes as well. There was made a conclusion about presence of posterior cranial fossa hypoplasia in all patients with hereditary syryngomyelia and in members of their families, both having MRT-features of Chiari malformation type I, and having no malformation. It was supposed that posterior cranial fossa hypoplasia is a neurovisual reflection of its hereditary phonotype, and the latter in some cases leads to cerebellar tonsil ptosis, and if there are some endogenic and exogenic factors — to development of family syringomyelia.

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A. V. Selezneva, E. G. Mendelevich, I. M. Mikhailov, L. R. Valieva, E. I. Bogdanov. MRT peculiarities of posterior cranial fossa in family syringomyelia. Neurology Bulletin, 2003, XXXV(1-2): 44-46 DOI:10.17816/nb89666

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Selezneva A.V., Mendelevich E.G., Mikhailov I.M., Valieva L.R., Bogdanov E.I.

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