Waardenburg syndrome

Waardenburg syndrome (WS) is a disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.

Synophrys

Meeting of the medial eyebrows in the midline.


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PMID (PMCID)
26114849
(4532278)
 FEMALE Middle Aged
Multimodal Ultrawide-Field Imaging Features in Waardenburg Syndrome.
Choudhry N, Rao RC.
Ophthalmic Surg Lasers Imaging Retina. 2015;46(6):670-3.
Waardenburg syndrome is characterized by a group of features including telecanthus, a broad nasal root, synophrys of the eyebrows, piedbaldism, heterochromia irides, and deafness.