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Jul 20, 2023 · Waardenburg syndrome refers to several rare genetic conditions that cause hearing loss, changes in the color of the eyes, skin, and hair, and changes in the shape of the face. A broad nasal...
Jun 6, 2017 · Waardenburg syndrome is a rare genetic condition that affects the color of a person’s skin, hair, and eyes. It can also cause hearing loss. There are four main types of Waardenburg syndrome.
- James Roland
Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes. Explore symptoms, inheritance, genetics of this condition.
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin.
Waardenburg syndrome is a genetic condition that causes changes to the coloring (pigmentation) of your hair, eyes and skin and can cause hearing loss in some people. Six genetic mutations cause the four types of Waardenburg syndrome, with each type categorized by its unique symptoms.
Albinism is usually obvious from a baby's appearance when they're born. Your baby's hair, skin and eyes may be examined to look for signs of missing pigment. As albinism can cause a number of eye problems, your baby may be referred to an eye specialist (ophthalmologist) for tests.
The 3 most common characteristics of Noonan syndrome are: unusual facial features; short stature (restricted growth) heart defects present at birth (congenital heart disease) Unusual facial features. People with Noonan syndrome may have a characteristic facial appearance, although this isn't always the case.
