Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy

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

Research output: Contribution to journalArticle

27 Citations (Scopus)

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
StatePublished - Mar 13 2001

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Brachial Plexus Neuritis
Genetic Heterogeneity
Chromosomes
Lod Score
Shoulder Pain
Brachial Plexus
Pedigree
Genetic Markers
Atrophy

ASJC Scopus subject areas

  • Neuroscience(all)

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.

Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy. / Watts, G. D J; O'Briant, K. C.; Borreson, T. E.; Windebank, Anthony John; Chance, Phillip F.

In: Neurology, Vol. 56, No. 5, 13.03.2001, p. 675-678.

Research output: Contribution to journalArticle

Watts, GDJ, O'Briant, KC, Borreson, TE, Windebank, AJ & Chance, PF 2001, 'Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy', Neurology, vol. 56, no. 5, pp. 675-678.
Watts GDJ, O'Briant KC, Borreson TE, Windebank AJ, Chance PF. Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy. Neurology. 2001 Mar 13;56(5):675-678.
Watts, G. D J ; O'Briant, K. C. ; Borreson, T. E. ; Windebank, Anthony John ; Chance, Phillip F. / Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy. In: Neurology. 2001 ; Vol. 56, No. 5. pp. 675-678.
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