A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state

At this stage in the development of medicine, there are difficulties in establishing the etiology of stroke in young patients. There are few significant risk factors from the group of metabolic hereditary diseases in the development of "young" strokes in the literature. This prompts the pu...

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Main Authors: N. V. Komissarova, A. A. Malkova, O. P. Potorochina, A. A. Ovchinnikova, P. O. Ivanina, D. O. Bayusheva
Format: Article
Language:Russian
Published: Private institution educational organization of higher education "Medical University "ReaViz" 2023-07-01
Series:Вестник медицинского института «Реавиз»: Реабилитация, врач и здоровье
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Online Access:https://vestnik.reaviz.ru/jour/article/view/708
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author N. V. Komissarova
A. A. Malkova
O. P. Potorochina
A. A. Ovchinnikova
P. O. Ivanina
D. O. Bayusheva
author_facet N. V. Komissarova
A. A. Malkova
O. P. Potorochina
A. A. Ovchinnikova
P. O. Ivanina
D. O. Bayusheva
author_sort N. V. Komissarova
collection DOAJ
description At this stage in the development of medicine, there are difficulties in establishing the etiology of stroke in young patients. There are few significant risk factors from the group of metabolic hereditary diseases in the development of "young" strokes in the literature. This prompts the publication of our observation. Aim: to describe a unique clinical case of "young" ischemic stroke in a 27-year-old woman whose daughter was diagnosed with type 2 gangliosidosis. To determine the cause of the stroke, the patient underwent DNA diagnostics, which showed a previously undescribed nucleotide sequence. A clinical case of ischemic stroke caused by a previously undescribed nucleotide sequence is presented.
format Article
id doaj-art-8657f2c9b2c04802ac2d8beea3875920
institution DOAJ
issn 2226-762X
2782-1579
language Russian
publishDate 2023-07-01
publisher Private institution educational organization of higher education "Medical University "ReaViz"
record_format Article
series Вестник медицинского института «Реавиз»: Реабилитация, врач и здоровье
spelling doaj-art-8657f2c9b2c04802ac2d8beea38759202025-08-20T03:20:01ZrusPrivate institution educational organization of higher education "Medical University "ReaViz"Вестник медицинского института «Реавиз»: Реабилитация, врач и здоровье2226-762X2782-15792023-07-0113312212610.20340/vmi-rvz.2023.3.CASE.3438A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous stateN. V. Komissarova0A. A. Malkova1O. P. Potorochina2A. A. Ovchinnikova3P. O. Ivanina4D. O. Bayusheva5Izhevsk State Medical Academy; Republican Clinical HospitalIzhevsk State Medical Academy; Republican Clinical HospitalRepublican Clinical HospitalIzhevsk State Medical AcademyIzhevsk State Medical AcademyIzhevsk State Medical AcademyAt this stage in the development of medicine, there are difficulties in establishing the etiology of stroke in young patients. There are few significant risk factors from the group of metabolic hereditary diseases in the development of "young" strokes in the literature. This prompts the publication of our observation. Aim: to describe a unique clinical case of "young" ischemic stroke in a 27-year-old woman whose daughter was diagnosed with type 2 gangliosidosis. To determine the cause of the stroke, the patient underwent DNA diagnostics, which showed a previously undescribed nucleotide sequence. A clinical case of ischemic stroke caused by a previously undescribed nucleotide sequence is presented.https://vestnik.reaviz.ru/jour/article/view/708gene mutationshereditary diseaseslysosomal storage diseasesgm1 gangliosidosisischemic stroke
spellingShingle N. V. Komissarova
A. A. Malkova
O. P. Potorochina
A. A. Ovchinnikova
P. O. Ivanina
D. O. Bayusheva
A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state
Вестник медицинского института «Реавиз»: Реабилитация, врач и здоровье
gene mutations
hereditary diseases
lysosomal storage diseases
gm1 gangliosidosis
ischemic stroke
title A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state
title_full A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state
title_fullStr A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state
title_full_unstemmed A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state
title_short A clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c.808T > C (p.Tyr270His of the GLBI gene (NM_ 000404.3, GMI-gangliosidosis type 2) in a heterozygous state
title_sort clinical case of ischemic stroke in a young patient with a previously undescribed nucleotide sequence c 808t c p tyr270his of the glbi gene nm 000404 3 gmi gangliosidosis type 2 in a heterozygous state
topic gene mutations
hereditary diseases
lysosomal storage diseases
gm1 gangliosidosis
ischemic stroke
url https://vestnik.reaviz.ru/jour/article/view/708
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