Dislocating medial triceps and ulnar neuropathy in three generations of one family.

Published

Journal Article

Variations in the medial triceps in conjunction with bilateral ulnar neuropathy have been identified in three generations of one family also possessing the phenotype of Waardenburg syndrome (a rare autosomal-dominant disorder with clinical features including cochlear deafness, dystopia canthorum, and pigmentation problems). To our knowledge, no other inherited condition with triceps anomalies has been reported. Study of this family provided insight into the relationship between dislocating medial triceps and ulnar neuropathy and demonstrated that a broad spectrum of clinical presentations exists-from being completely asymptomatic to producing symptomatic snapping and ulnar neuropathy.

Full Text

Duke Authors

Cited Authors

  • Spinner, RJ; Davids, JR; Goldner, RD

Published Date

  • January 1997

Published In

Volume / Issue

  • 22 / 1

Start / End Page

  • 132 - 137

PubMed ID

  • 9018626

Pubmed Central ID

  • 9018626

Electronic International Standard Serial Number (EISSN)

  • 1531-6564

International Standard Serial Number (ISSN)

  • 0363-5023

Digital Object Identifier (DOI)

  • 10.1016/s0363-5023(05)80193-5

Language

  • eng