Keyword Analysis & Research: what is waardenburg syndrome
Keyword Research: People who searched what is waardenburg syndrome also searched
Search Results related to what is waardenburg syndrome on Search Engine
-
Waardenburg Syndrome: Symptoms & Causes - Cleveland Clinic
https://my.clevelandclinic.org/health/diseases/24012-waardenburg-syndrome
WEBOverview. What is Waardenburg syndrome? 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. Advertisement.
DA: 42 PA: 86 MOZ Rank: 55
-
Waardenburg Syndrome: Symptoms, Treatment, and More - Healthline
https://www.healthline.com/health/waardenburg-syndrome
WEBJun 5, 2017 · Diagnosis. Treatment. Outlook. What is Waardenburg syndrome? Waardenburg syndrome is a rare genetic condition that affects the color of a person’s skin, hair, and...
DA: 91 PA: 9 MOZ Rank: 17
-
Waardenburg syndrome - Wikipedia
https://en.wikipedia.org/wiki/Waardenburg_syndrome
WEBWaardenburg 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.
DA: 100 PA: 15 MOZ Rank: 93
-
Waardenburg syndrome - About the Disease - Genetic and Rare …
https://rarediseases.info.nih.gov/diseases/5525/waardenburg-syndrome/
WEBSummary. Waardenburg syndrome (WS) is a group of genetic conditions characterized by varying degrees of hearing loss and differences in the coloring (pigmentation) of the eyes, hair, and skin. Signs and symptoms can vary both within and between families. Various other features may also be present.
DA: 36 PA: 20 MOZ Rank: 58
-
Waardenburg Syndrome - Symptoms, Causes, Treatment | NORD
https://rarediseases.org/rare-diseases/waardenburg-syndrome/
WEBMay 21, 2015 · Disease Overview. Waardenburg syndrome is a genetic disorder that may be evident at birth (congenital). The range and severity of associated symptoms and findings may vary greatly from case to case.
DA: 95 PA: 59 MOZ Rank: 48
-
Waardenburg syndrome: Types, symptoms, and causes - Medical News Today
https://www.medicalnewstoday.com/articles/320549
WEBJan 8, 2018 · 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...
DA: 16 PA: 77 MOZ Rank: 82
-
Waardenburg syndrome: MedlinePlus Genetics
https://medlineplus.gov/genetics/condition/waardenburg-syndrome/
WEBDescription. 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.
DA: 1 PA: 22 MOZ Rank: 61
-
Waardenburg Syndrome: What Is It, Causes, Diagnosis, and More …
https://www.osmosis.org/answers/waardenburg-syndrome
WEBMay 25, 2023 · Waardenburg syndrome is a rare congenital disease involving a group of genetic conditions, including distinctive facial features, discoloration of various body parts, and congenital hearing loss. The range and severity of associated findings may be highly variable, even among affected members of the same family.
DA: 22 PA: 14 MOZ Rank: 45
-
Waardenburg syndrome Information | Mount Sinai - New York
https://www.mountsinai.org/health-library/diseases-conditions/waardenburg-syndrome
WEBWaardenburg syndrome is a group of conditions passed down through families. The syndrome involves deafness and pale skin, hair, and eye color. Causes. Waardenburg syndrome is most often inherited as an autosomal dominant trait. This means only one parent needs to pass on the altered gene for a child to have this condition.
DA: 87 PA: 40 MOZ Rank: 73
-
Waardenburg Syndrome - StatPearls - NCBI Bookshelf
https://www.ncbi.nlm.nih.gov/books/NBK560879/
WEBJul 4, 2023 · Waardenburg syndrome (WS) is a group of genetic conditions inherited in an autosomal dominant fashion.[1] It is named after Dutch ophthalmologist and geneticist Petrus Johannes Waardenburg, who described it in 1951.[1] During embryogenesis, there is an abnormal distribution of melanocytes, which results in patchy areas of depigmentation.
DA: 74 PA: 28 MOZ Rank: 24
