PT - JOURNAL ARTICLE AU - A E Harding AU - C M Hall AU - M Baraitser TI - Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia) AID - 10.1136/jmg.19.2.110 DP - 1982 Apr 01 TA - Journal of Medical Genetics PG - 110--115 VI - 19 IP - 2 4099 - http://jmg.bmj.com/content/19/2/110.short 4100 - http://jmg.bmj.com/content/19/2/110.full SO - J Med Genet1982 Apr 01; 19 AB - A syndrome characterised by asymmetrical radial dysplasia, dysmorphic facies, conductive deafness, and external ear deformity is described in a mother and her daughter. This combination of anomalies has previously been reported in members of a single family. The disorder appears to be clinically and genetically distinct from others associated with radial dysplasia, such as Nager's acrofacial dysostosis and the lachrimoauriculoradiodental syndrome. Inheritance is autosomal dominant, with marked variation in expression of the mutant gene.