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https://rarediseases.info.nih.gov/diseases/5525/waardenburg-syndrome/cases/55219
Feb 11, 2016 · A diagnosis of Waardenburg syndrome (WS) is made based on the presence of signs and symptoms. In 1992, the Waardenburg Consortium proposed diagnostic criteria, which includes both major and minor criteria. A diagnosis of WS type 1 (the most common type) needs 2 major, or 1 major and 2 minor of the following criteria: Major criteria:
https://rarediseases.info.nih.gov/diseases/5524/waardenburg-syndrome-type-4
Apr 18, 2011 · Waardenburg syndrome type 4, also known as Waardenburg-Shah syndrome, is a genetic condition that can cause hearing loss; changes in coloring (pigmentation) of the hair, skin, and eyes; and Hirschsprung disease, an intestinal disorder that causes severe constipation or blockage of the intestine.Waardenburg syndrome type 4 is further divided into types 4A, 4B, and 4C based on their …
https://www.verywellhealth.com/four-types-symptoms-waardenburg-syndrome-2860498
Nov 23, 2019 · Waardenburg syndrome is divided into four types, based on the physical manifestations of the condition. Individuals are considered to have Waardenburg syndrome type 1 if they have 2 major or 1 major plus 2 minor criteria. Waardenburg syndrome type 2 is defined as having all the features of type 1 except dystopia canthorum.
https://ghr.nlm.nih.gov/condition/waardenburg-syndrome
Oct 01, 2019 · Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes. Although most people with Waardenburg syndrome have normal hearing, moderate to profound hearing loss can occur in one or both ears. The hearing loss is present from birth (congenital). People with this condition often have very pale blue …
https://www.ncbi.nlm.nih.gov/books/NBK1531/
Jul 30, 2001 · Waardenburg syndrome type I (WS1) is an auditory-pigmentary disorder comprising congenital sensorineural hearing loss and pigmentary disturbances of the iris, hair, and skin, along with dystopia canthorum (lateral displacement of the inner canthi). The hearing loss in WS1, observed in approximately 60% of affected individuals, is congenital, typically non-progressive, either unilateral or ...Cited by: 18
https://en.wikipedia.org/wiki/Waardenburg_syndrome
Waardenburg syndrome is a rare genetic condition 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.Specialty: Medical genetics
https://www.facebook.com/waardenburg
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