People with this condition often have very pale blue eyes or different colored eyes, such as one blue eye and one brown eye. Sometimes one eye has segments of two different colors. Distinctive hair coloring (such as a patch of white hair or hair that prematurely turns gray) is another common sign of the condition.
Aug 16, 2022
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Aug 15, 2022 · Waardenburg syndrome is a genetic condition that affects the coloring (pigmentation) of your skin, hair and eyes.
Symptoms · Cleft lip (rare) · Constipation · Deafness (more common in type II disease) · Extremely pale blue eyes or eye colors that don't match ( heterochromia ) ...
Waardenburg syndrome
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, a white forelock or patches of light skin. Wikipedia
Parent Disease: Genetic disorder
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies.
A broad nasal root can cause the appearance of wide-set eyes. Researchers have identified four distinct types of the syndrome, though there may be additional ...
It clinically presents as depigmentation of skin and hairs with a change of eye color. Vogt-Koyanagi-Harada disease: Usually affects the skin, eyes, ear, and ...
For example, Waardenburg syndrome type I (WS1) is characteristically associated with sideways displacement of the inner angles of the eyes (i.e., dystopia ...
Waardenburg syndrome is a rare genetic disorder characterised by sensorineural hearing loss and pigmentary abnormalities of the hair, skin, and eyes.
Jul 23, 2020 · Waardenburg syndrome (WS) is a rare genetic disorder characterized by various degrees of deafness, abnormal pigmentation and minor defects in ...
People with this condition often have very pale blue eyes or different colored eyes, such as one blue eye and one brown eye. Sometimes one eye has segments of ...
