Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25.

doi:10.1007/s004390050430

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Article

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25.

Human genetics - 1 May 1997

Stögbauer F, Young P, Timmerman V, Spoelders P, Ringelstein E B, Van Broeckhoven C, Kurlemann G

Abstract excerpt

Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant, recurrent focal neuropathy characterized by episodes of painful brachial plexus neuropathy with muscle weakness and atrophy, as well as sensory disturbances. Single episodes are commonly preceded by unspecific infections or immunizat...

Topics

Brachial Plexus Neuritis
Chromosome Mapping
Chromosomes, Human, Pair 17
DNA Primers
Dinucleotide Repeats
Female
Genes, Dominant
Genetic Linkage
Genetic Markers
Genotype
Germany
Humans
Lod Score
Male
Pedigree
Polymerase Chain Reaction
Turkey

Source

Open in PubMed

Identifiers

PMID: 9150742
DOI: 10.1007/s004390050430

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9150742-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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