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Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophic.

Authors :
Rattay TW
Just J
Röben B
Hengel H
Schüle R
Synofzik M
Söhn AS
Winter N
Dammeier N
Schöls L
Grimm A
Source :
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2018 Nov 03; Vol. 13 (1), pp. 194. Date of Electronic Publication: 2018 Nov 03.
Publication Year :
2018

Abstract

Objective: High-resolution nerve ultrasound (HRUS) is a painless tool to quickly evaluate peripheral nerve morphology in vivo. This study set out to characterize peripheral nerve involvement in X-linked adrenomyeloneuropathy (AMN) by HRUS.<br />Methods: Thirteen adults with genetically proven AMN were examined using the Ultrasound pattern sum score (UPSS) to evaluate morphological abnormalities of peripheral nerves, vagal nerves, as well as cervical nerve roots. Ultrasound results were correlated with clinical findings and nerve conduction studies.<br />Results: UPSS was increased in six out of 13 patients. Nerve enlargement was mostly inhomogeneous and regional. The median, ulnar, and vagal nerves presented with more prominent alterations than nerves of the lower limbs. The proximal-to-distal ratio was significantly enlarged for the median nerve. HRUS findings matched nerve conduction studies, but identified one patient with enlarged nerves and yet normal conduction velocities. Sonographic findings did not correlate with disease duration or disease severity as assessed by the spastic paraplegia rating scale.<br />Conclusion: HRUS reveals significant multifocal regional nerve swellings with reduced echo intensity as the morphological equivalent of electrophysiological peripheral nerve affection in AMN patients. Ultrasound and NCS characteristics in AMN seem to differ from other demyelinating neuropathies like CIDP or CMT1a.<br />Trial Registration: German clinical-trial-register (DRKS) ( DRKS-ID 00005253 ) Registered 15 October 2013.

Details

Language :
English
ISSN :
1750-1172
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Orphanet journal of rare diseases
Publication Type :
Academic Journal
Accession number :
30390710
Full Text :
https://doi.org/10.1186/s13023-018-0939-7