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Article

Recurrent polyradiculoneuropathy with the 17p11.2 deletion.

Muscle & nerve - 1 Sept 1997

Le Forestier N, LeGuern E, Coullin P, Birouk N, Maisonobe T, Brice A, Léger J M, Bouche P

Abstract excerpt

Hereditary neuropathy with liability to pressure palsies (HNPP) classically occurs as recurrent focal neuropathy. We report the first known instance of HNPP manifesting, over a 15-year period, as a recurrent sensorimotor polyneuropathy and confirmed by the presence of the PMP-22 gene deletion. We suggest that the molecular study of the 17p11.2 region could be an effective non invasive investigative tool in cases...

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Share to Chromosomes, Human, Pair 17
Share to Gene Deletion
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9270678
DOI: 10.1002/(sici)1097-4598(199709)20:9<1184::aid-mus16>3.0.co;2-t

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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