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Verfasst von:Godel, Tim [VerfasserIn]   i
 Cossel, Katharina von [VerfasserIn]   i
 Friedrich, Reinhard E. [VerfasserIn]   i
 Glatzel, Markus [VerfasserIn]   i
 Canaan-Kühl, Sima [VerfasserIn]   i
 Duning, Thomas [VerfasserIn]   i
 Kronlage, Moritz [VerfasserIn]   i
 Heiland, Sabine [VerfasserIn]   i
 Bendszus, Martin [VerfasserIn]   i
 Muschol, Nicole [VerfasserIn]   i
 Mautner, Victor-Felix [VerfasserIn]   i
Titel:Assessment of peripheral nervous system alterations in patients with the Fabry telated GLA-variant p.A143T
Verf.angabe:Tim Godel, Katharina von Cossel, Reinhard E. Friedrich, Markus Glatzel, Sima Canaan-Kühl, Thomas Duning, Moritz Kronlage, Sabine Heiland, Martin Bendszus, Nicole Muschol and Victor-Felix Mautner
E-Jahr:2020
Jahr:30 November 2020
Umfang:11 S.
Fussnoten:Gesehen am 09.02.2022
Titel Quelle:Enthalten in: Diagnostics
Ort Quelle:Basel : MDPI, 2011
Jahr Quelle:2020
Band/Heft Quelle:10(2020), 12, Artikel-ID 1027, Seite 1-11
ISSN Quelle:2075-4418
Abstract:The purpose of this study is to examine alterations of the peripheral nervous system (PNS) in oligo-symptomatic patients carrying the Fabry related GLA-gene variant p.A143T by Magnetic Resonance Neurography (MRN) and skin biopsy. This prospective study assessed dorsal root ganglia (DRG) volume L3 to S2, vascular permeability of the DRG L5, S1, and the spinal nerve L5 in five patients carrying p.A143T in comparison to patients with classical Fabry mutations and healthy controls. Moreover, skin punch biopsies above the lateral malleolus of the right foot were obtained in four patients and intraepidermal nerve fiber density (IENFD) was counted individually. Compared to controls, DRG volumes of p.A143T patients were enlarged by 30% (L3, p < 0.05), 35% (L4, p < 0.05), 29% (L5, p = 0.15), 36% (S1, p < 0.01), and 18% (S2, p < 0.05), but less pronounced compared to patients carrying a classical Fabry mutation. Compared to healthy controls, vascular permeability was decreased by 40% (L5 right), 49% (L5 left), 48% (S1 right), and 49% (S1) (p < 0.01-p < 0.001), but non-significant less than patients carrying a classical Fabry mutation. Compared to sex-matched 5% lower normative reference values per decade, IENFD was decreased in three of four patients. MRN and determination of IENFD is able to detect early alteration of the PNS segment in oligo-symptomatic patients with the disease-modifying GLA-variant p.A143T on an individual basis. This procedure might also help in further GLA-variants of uncertain significance for early identification of patients with single major organ manifestation.
DOI:doi:10.3390/diagnostics10121027
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.3390/diagnostics10121027
 Volltext: https://www.mdpi.com/2075-4418/10/12/1027
 DOI: https://doi.org/10.3390/diagnostics10121027
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:dorsal root ganglia
 Fabry disease
 Magnetic Resonance Neurography
 neuropathic pain
 peripheral neuropathy
K10plus-PPN:1788786580
Verknüpfungen:→ Zeitschrift

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