| Literature DB >> 6601715 |
P Strisciuglio, V Raia, A Di Meo, E Rinaldi, G Andria.
Abstract
A 15-year-old female was found to have the typical features of Wildervanck's syndrome, including Klippel-Feil anomaly, abducens paralysis, retraction of the bulbi, and deafness. In addition, she had bilateral lens subluxation and facial paralysis, neither of which have been reported in patients with Wildervanck's syndrome.Entities:
Mesh:
Year: 1983 PMID: 6601715 PMCID: PMC1048993 DOI: 10.1136/jmg.20.1.72
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318