| Waardenburg syndrome |
Congenital genetic disorder which varies across individuals. Characteristics may include facial abnormalities, irises of different colors, diminished coloration of the hair and skin, white forelock, wide nasal bridge, and a sensorineural hearing loss.
Ãâó: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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| Waardenburg syndrome |
a combination of symptoms that include hereditary deafness, appearance of a broad nasal bridge, different colored eyes, and a streak of white hair in the middle of the forehead
Ãâó: www.hearingcenteronline.com/diction_vw.shtml
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| Waardenburg's s. |
1. an autosomal dominant disorder characterized by wide bridge of the nose due to lateral displacement of the inner canthi and puncta, pigmentary disturbances, including white forelock, heterochromia iridis, white eyelashes, leukoderma, and sometimes cochlear hearing loss. 2. an autosomal dominant disorder characterized by acrocephaly, orbital and facial deformities, and brachydactyly with mild soft tissue syndactyly; cleft palate, hydrophthalmos, cardiac malformation, and contractures of the elbows and knees may also be present. Called also Klein-Waardenburg s.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Waardenburg's syndrome |
see under syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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