Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy

G. D.J. Watts, K. C. O'Briant, T. E. Borreson, A. J. Windebank, Phillip F. Chance

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

Hereditary neuralgic amyotrophy (HNA) is a rare autosoreal dominant disorder characterized by recurrent episodes of severe arm and shoulder pain with weakness, atrophy, and sensory impairment in a brachial plexus distribution. Recent studies mapped the HNA locus to chromosome 17q25. Two pedigrees with clinically typical HNA in which markers from chromosome 17q25 do not cosegregate with the disease and in which lod scores do not support linkage to chromosome 17q25 were identified.

Original languageEnglish (US)
Pages (from-to)675-678
Number of pages4
JournalNeurology
Volume56
Issue number5
DOIs
StatePublished - Mar 13 2001

ASJC Scopus subject areas

  • Clinical Neurology

Fingerprint Dive into the research topics of 'Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy'. Together they form a unique fingerprint.

  • Cite this

    Watts, G. D. J., O'Briant, K. C., Borreson, T. E., Windebank, A. J., & Chance, P. F. (2001). Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy. Neurology, 56(5), 675-678. https://doi.org/10.1212/WNL.56.5.675