Searching for Waardenburg Syndrome Support information? Find all needed info by using official links provided below.
https://rarediseases.info.nih.gov/diseases/5525/waardenburg-syndrome
45 rows · Feb 10, 2016 · Waardenburg syndrome (WS) is a group of genetic conditions characterized …
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).
https://rarediseases.info.nih.gov/diseases/5525/waardenburg-syndrome/cases/55219
Feb 11, 2016 · Yes. People can have Waardenburg syndrome (WS) without having some type of heterochromia iridis.In general, heterochromia iridis is less common in affected people than the hair and skin features of WS. In WS type 1 for example, heterochromia iridis is present in 15%-31% of affected people, and hypoplastic blue irides is present in 15%-18% of affected people.
https://medlineplus.gov/ency/article/001428.htm
Waardenburg syndrome is most often inherited as an autosomal dominant trait. This means only one parent has to pass on the faulty gene for a child to be affected. There are four main types of Waardenburg syndrome. The most common are type I and type II. Type III (Klein-Waardenburg syndrome) and type IV (Waardenburg-Shah syndrome) are rarer.
https://www.medicalnewstoday.com/articles/320549.php
Jan 08, 2018 · A person with Waardenburg syndrome may need support to manage their condition, particularly if it affects their appearance in ways that are not …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1051028/
Type III WS (Klein-Waardenburg syndrome, with abnormalities of the arms) is an extreme presentation of type I; some but not all patients are homozygotes. Type IV WS (Shah-Waardenburg syndrome with Hirschsprung disease) can be caused by mutations in the genes for endothelin-3 …
https://www.mdjunction.com/waardenburg-syndrome
The Waardenburg Syndrome Support Group is a community of patients, family members and friends dedicated to dealing with Waardenburg Syndrome, together.
https://www.dermatologyadvisor.com/home/decision-support-in-medicine/dermatology/waardenburgs-syndrome/
Waardenburg syndrome (ICD-9-CM 270.2) Are You Confident of the Diagnosis? Waardenburg’s syndrome (WS) was first described in 1951 by Waardenburg, a Dutch ophthalmologist. It is an autosomal dominant genetic disorder characterized by piebaldism (congenital poliosis and leukoderma), pigmentary abnormalities of the iris, lateral displacement of the inner canthi of the eyes (dystopia canthorum ...
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