File:Waardenburg syndrome.jpg
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Summary
| Description |
Français : Le syndrome de Waardenburg est une maladie génétique de transmission autosomique dominante associant une surdité avec des anomalies de la pigmentation de la peau ou des cheveux ou de l’iris.
Si un individu présente un état homozygote pour l’allèle provoquant le syndrome de Waardenburg, il y a mort au stade fœtal. Quatre types de ce syndrome existent (très probablement chacune associée à un type de mutation génétique). Ils font encore l'objet d'études, dont génétiques et en biologie moléculaire afin de mieux les cerner et en comprendre plus finement |
| Date | |
| Source | Own work |
| Author | Mohammad2018 |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 07:35, 18 June 2023 | | 688 × 1,020 (191 KB) | Sciencia58 | so |
| 22:21, 20 April 2018 |  | 690 × 1,255 (553 KB) | Mohammad2018 | User created page with UploadWizard |
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