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Article

Hereditary neuropathy with liability to pressure palsy.

Folia neuropathologica - 1 Jan 2006

Paprocka Justyna, Kajor Maciej, Jamroz Ewa, Jezela-Stanek Aleksandra, Seeman Pavel, Marszał Elzbieta

Abstract excerpt

Hereditary neuropathy with liability to pressure palsy (HNPP) is an autosomal dominant disease with sensory and motor nerve palsies usually precipitated by trivial trauma or compression. In the majority of cases HNPP is caused by deletion of the peripheral myelin protein 22 gene (PMP22) on chromosome 17p11.2. The authors present a family case with genetically proven HNPP.

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Source

Identifiers

PMID: 17183456

Genes

PMP22

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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Hereditary neuropathy with liability to pressure palsy.PMID 17183456Read ↗

Hereditary neuropathy with liability to pressure palsy: a brief review with a case report.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy: an investigation in a rare and large Chinese family.Semantic proximity Read ↗

Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy in childhood.Semantic proximity Read ↗

[Hereditary neuropathy with liability to pressure palsies in childhood: Report of three cases].Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsies: description of seven patients without known family history.Semantic proximity Read ↗

[Hereditary neuropathy with liability to pressure palsies caused by 17p11.2 chromosome deletion].Semantic proximity Read ↗

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

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