| WS | Waardenburg syndrome; ward secretary; Warkany syndrome; Warthin-Starry [stain]; water soluble; water... |
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| WSI | Waardenburg syndrome type I |
| WS | Waardenburg Syndrome |
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| WS1 | Waardenburg syndrome Type I |
| Waardenburg syndrome | <syndrome> Rare, autosomal dominant disease with variable penetrance and several known clinical types. Clinical features include depigmentation of the skin and hair with a white forelock, congenital cochlear deafness, heterochromia iridis or hypochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root producing increased width of the root of the nose, dystopia canthorum, lateral dystopia of medial canthi and lacrimal puncta and synophrys. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-waardenburg syndrome refers to a disorder that also includes upper limb abnormalities. Inheritance: audosomal dominant. (21 Jun 2000) |
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| Waardenburg, Petrus Johannes | <person> Dutch ophthalmologist, 1886-1979. See: Waardenburg syndrome. (05 Mar 2000) |
Synonyms : Klein's Syndrome, Waardenburg-Klein Syndrome, Klein Syndrome, Klein Waardenburg Syndrome, Kleins Syndrome, Syndrome, Klein's, Syndrome, Klein-Waardenburg, Syndrome, Waardenburg's, Syndrome, Waardenburg-Klein, Waardenburg Klein Syndrome, Waardenburg Syndrome
| 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.
출처: 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
출처: 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.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Waardenburg's syndrome |
see under syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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