[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 35.153.39.7. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
December 1962

Waardenburg's Syndrome: A Variation of the First Arch Syndrome

Author Affiliations

LOS ANGELES

From the Department of Dermatology and the Department of Pediatrics, White Memorial Hospital and Loma Linda University.

Arch Dermatol. 1962;86(6):718-724. doi:10.1001/archderm.1962.01590120016003
Abstract

The first arch syndrome is a group of conditions in which anatomical and physiological abnormalities are found in the area supplied by the vessels of the first visceral arch in early embryonic life. Anomalies of the first visceral arch produce the defects of the syndrome by modifications of the blood supply to the rapidly growing and differentiating embryonic tissues. The disease is hereditary. Waardenburg's syndrome consists of deafness, heterochromia, a white forelock, and various anatomical changes. An unusual case is presented, showing extensive partial albinism in addition to many of the stigmata of Waardenburg's syndrome. Genetic and nutritional factors in relation to the first arch syndrome are discussed.

×