waardenburg syndrome | Waardenburg syndrome

Keyword	CPC	PCC	Volume	Score	Length of keyword
waardenburg syndrome	1.61	1	3988	41	20
waardenburg	0.82	0.2	7409	73	11
syndrome	0.24	0.9	8164	22	8

Keyword	CPC	PCC	Volume	Score
waardenburg syndrome	1.08	0.3	8631	22
waardenburg syndrome eyes	0.37	0.2	5484	31
waardenburg syndrome symptoms	0.7	0.7	3352	1
waardenburg syndrome type 2	0.9	0.1	956	87
waardenburg syndrome type 1	0.66	0.8	4728	54
waardenburg syndrome icd 10	0.45	0.2	6526	89
waardenburg syndrome celebrities	1.07	0.5	1434	44
waardenburg syndrome genereviews	0.54	0.1	7121	88
waardenburg syndrome type 3	1.53	0.9	3432	38
waardenburg syndrome type 4	1.54	0.2	2879	65
waardenburg syndrome types	0.28	0.8	7966	77
waardenburg syndrome pictures	1.83	0.2	2884	42
waardenburg syndrome genetics	1.97	0.2	9382	4
waardenburg syndrome hearing loss	0.7	1	6071	61
waardenburg syndrome type 2a	1.06	0.5	4731	5
waardenburg syndrome anna joy taylor	1.29	0.5	488	82
what is waardenburg syndrome	1.57	0.8	7250	89
klein waardenburg syndrome	0.34	0.3	6396	88
famous people with waardenburg syndrome	1.22	0.7	8967	13

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Waardenburg syndrome - Wikipedia
wikipedia.org

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 …

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Waardenburg Syndrome: Symptoms & Causes - Cleveland Clinic
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/24012-waardenburg-syndrome

WEBWaardenburg syndrome is a genetic condition that affects the coloring (pigmentation) of your skin, hair and eyes. This condition can also cause hearing loss. In rare cases, Waardenburg syndrome can cause constipation or intestinal blockages. Treatment is available to alleviate symptoms but isn’t necessary for all types of the condition.

DA: 90 PA: 23 MOZ Rank: 16

Waardenburg Syndrome - Symptoms, Causes, Treatment | NORD
rarediseases.org

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. However, primary features often include distinctive facial abnormalities; unusually diminished coloration (pigmentation) of the …

DA: 52 PA: 54 MOZ Rank: 41

Waardenburg syndrome - About the Disease - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/5525/waardenburg-syndrome/

WEBWaardenburg 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: 21 PA: 45 MOZ Rank: 91

Waardenburg syndrome: Types, symptoms, and causes - Medical News Today
medicalnewstoday.com

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 the shape of...

DA: 61 PA: 42 MOZ Rank: 84

Waardenburg syndrome Information | Mount Sinai - New York
mountsinai.org

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: 10 PA: 65 MOZ Rank: 2

Waardenburg Syndrome - StatPearls - NCBI Bookshelf
nih.gov

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: 66 PA: 50 MOZ Rank: 43

Waardenburg syndrome: MedlinePlus Genetics
medlineplus.gov

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: 9 PA: 23 MOZ Rank: 63

Waardenburg Syndrome: Symptoms, Treatment, and More - Healthline
healthline.com

https://www.healthline.com/health/waardenburg-syndrome

WEBJun 5, 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...

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Orphanet: Waardenburg syndrome
orpha.net

https://www.orpha.net/en/disease/detail/3440

WEBWaardenburg syndrome (WS) is a disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes. ORPHA:3440. Classification level: Disorder. Prevalence: 1-9 / 100 000.

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