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Proton MR spectroscopy in three children with Tay-Sachs disease
Tay-Sachs disease is an inherited metabolic disease caused by the accumulation of GM(2) gangliosides in the central nervous system. Deficiency of hexosaminidase A leads to the accumulation of gangliosides in neurons, axons and glial cells. To present the cranial MRI and proton MR spectroscopy findin...
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Published in: | Pediatric radiology 2005-11, Vol.35 (11), p.1081-1085 |
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creator | Aydin, Kubilay Bakir, Baris Tatli, Burak Terzibasioglu, Ege Ozmen, Meral |
description | Tay-Sachs disease is an inherited metabolic disease caused by the accumulation of GM(2) gangliosides in the central nervous system. Deficiency of hexosaminidase A leads to the accumulation of gangliosides in neurons, axons and glial cells.
To present the cranial MRI and proton MR spectroscopy findings of children of Tay-Sachs disease.
Three children aged 10, 20 and 21 months were examined.
On T2-weighted MR images there were hyperintense signal changes in the basal ganglia and cerebral white matter. MR spectroscopy demonstrated an increase in myoinositol/creatine and choline/creatine ratios with a decrease in the N-acetyl aspartate/creatine ratio.
The spectroscopy findings support demyelination, gliosis and neuronal loss in the neuropathological process of Tay-Sachs disease. |
doi_str_mv | 10.1007/s00247-005-1542-3 |
format | article |
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To present the cranial MRI and proton MR spectroscopy findings of children of Tay-Sachs disease.
Three children aged 10, 20 and 21 months were examined.
On T2-weighted MR images there were hyperintense signal changes in the basal ganglia and cerebral white matter. MR spectroscopy demonstrated an increase in myoinositol/creatine and choline/creatine ratios with a decrease in the N-acetyl aspartate/creatine ratio.
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To present the cranial MRI and proton MR spectroscopy findings of children of Tay-Sachs disease.
Three children aged 10, 20 and 21 months were examined.
On T2-weighted MR images there were hyperintense signal changes in the basal ganglia and cerebral white matter. MR spectroscopy demonstrated an increase in myoinositol/creatine and choline/creatine ratios with a decrease in the N-acetyl aspartate/creatine ratio.
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Deficiency of hexosaminidase A leads to the accumulation of gangliosides in neurons, axons and glial cells.
To present the cranial MRI and proton MR spectroscopy findings of children of Tay-Sachs disease.
Three children aged 10, 20 and 21 months were examined.
On T2-weighted MR images there were hyperintense signal changes in the basal ganglia and cerebral white matter. MR spectroscopy demonstrated an increase in myoinositol/creatine and choline/creatine ratios with a decrease in the N-acetyl aspartate/creatine ratio.
The spectroscopy findings support demyelination, gliosis and neuronal loss in the neuropathological process of Tay-Sachs disease.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>16079982</pmid><doi>10.1007/s00247-005-1542-3</doi><tpages>5</tpages></addata></record> |
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subjects | Brain - metabolism Brain - pathology Female Humans Infant Magnetic Resonance Imaging - methods Magnetic Resonance Spectroscopy - methods Male Neurotransmitter Agents - metabolism Protons Tay-Sachs Disease - diagnosis Tay-Sachs Disease - metabolism |
title | Proton MR spectroscopy in three children with Tay-Sachs disease |
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