Early and progressive microstructural damage is present in Fabry disease.

<p>In (a), a comparison of FLAIR histograms using the normalized signal intensity (nSI) from the age-based first and fourth quartiles of healthy controls. The histograms for the FLAIR nSI from the younger adult Fabry and control cohorts are shown in (b). Similar comparisons using histograms fr...

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التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Jacob W. Johnson (20172850) (author)
مؤلفون آخرون:	Hediyeh Baradaran (9861244) (author), Jubel Morgan (476471) (author), Henrik Odèen (22633876) (author), Emma Friel (22633879) (author), Carrie Bailey (7009100) (author), Brandon A. Zielinski (17051076) (author), Hunter R. Underhill (3151677) (author)
منشور في:	2025
الموضوعات:	Medicine Cell Biology Neuroscience Physiology Developmental Biology Mental Health Biological Sciences not elsewhere classified wml severity increased identify factors unique g ., fluid flair ), semi enzyme replacement therapy diffusion tensor imaging corpus callosum atrophied causes glycolipid accumulation became statistically significant attenuated inversion recovery 8 – 63 serial cognitive assessments progressive tissue damage common neurologic sequelae typical brain aging related brain alterations related cognitive decline older fabry patients white matter lesions median age 36 matched healthy controls div >< p using quantitative mri used structural mri younger fabry participants cognitive decline white matter quantitative mri structural mris participants underwent neurologic diseases microstructural damage mri study mri ). fabry drives fabry disease compared fabry rare x phenomena absent p </ normal age neuroradiologist ’ neurocognitive assessment lysosomal alpha linked deficiency large population insidious degeneration impaired cognition highly prevalent fisher ’
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Early and progressive microstructural damage is present in Fabry disease.

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