- Waardenburg syndrome
- Waardenburg syndrome.См. синдром Ваарденбурга.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
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Waardenburg syndrome
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Waardenburg syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 14021 DiseasesDB mult= DiseasesDB2|33475 ICD10 = ICD10|E|70|3|e|70 (ILDS E70.32) ICD9 = ICD9|270.2 ICDO = OMIM = OMIM mult = MedlinePlus = 001428 eMedicineSubj = ped eMedicineTopic = 2422… … Wikipedia
Waardenburg syndrome (WS) — An hereditary disorder characterized by hearing impairment, a white forelock (a frontal white blaze of hair), a difference of color between the iris of one eye and the other (heterochromia iridis), white eye lashes, wide set inner corners of the… … Medical dictionary
Waardenburg syndrome — Waar·den·burg syndrome (vahrґden boorg) [Petrus Johannes Waardenburg, Dutch ophthalmologist, 1886–1979] see under syndrome … Medical dictionary
Waardenburg syndrome — any of several hereditary conditions characterized principally by a combination of auditory and pigmentary abnormalities, including hypopigmented or heterochromatic irides and sometimes hypopigmented fundi; pigmentation defects of the skin and… … Medical dictionary
Klein-Waardenburg syndrome — Klein Waar·den·burg syndrome (klīnґ vahrґdən bərg) [David Klein, Swiss ophthalmologist, 1908–1993; Petrus Johannes Waardenburg, Dutch ophthalmologist, 1886–1979] Waardenburg syndrome type 3; see under syndrome … Medical dictionary
Shah-Waardenburg syndrome — Shah Waar·den·burg syndrome (shahґ vahrґden boorg) [Krishnakumar N. Shah, Indian physician, late 20th century; Petrus Johannes Waardenburg, Dutch ophthalmologist, 1886–1979] Waardenburg syndrome type 4; see under syndrome … Medical dictionary
Klein-Waardenburg syndrome — Waardenburg s. type 3 … Medical dictionary
Shah-Waardenburg syndrome — Waardenburg s. type 4 … Medical dictionary
Syndrome de waardenburg type 1 — Autre nom {{{Autre nom}}} Référence MIM … Wikipédia en Français
Syndrome de Waardenburg type 1 — Référence MIM 193500 Transmission Dominante Chromosome 2q35 Gène PAX3 Mutation Ponctuelle … Wikipédia en Français
