Klein syndrome 6

General: Autosomal dominant; belongs to the group of iridodermatoauditive dysplasias.

Ocular: Hypertelorism; blepharophimosis; hypertrichosis; blue irides; heterochromia.

Clinical: Bilateral labyrinthine deafness; mandibular retrognathism; skull deformities and arched palate; partial albinism of skin and hair; syndactylism (cutaneous).

Duke-Elder S, ed. System of Ophthalmology, vol. III, part 2. St. Louis: CV Mosby, 1964.

Klein D. Albinisme Partiel (Leucisme), Accomne de Surdi-mutite, d'Osteomyodysplasie, de Raideurs Articulaires Congenitales Multiples et d'Autres Malformations Congenitales. Arch Julius Klaus Stift Vererb Forsch 1947; 22:336, and Helv Paediatr Acta 1950; 5:38.