williams syndrome | Williams syndrome

Keyword	CPC	PCC	Volume	Score	Length of keyword
williams syndrome	1.31	1	1953	74	17
williams	1.06	0.5	9601	25	8
syndrome	1.33	0.2	1331	60	8

Keyword	CPC	PCC	Volume	Score
williams syndrome	1.86	0.7	8902	72
williams syndrome definition	0.5	0.1	7243	36
williams syndrome symptoms	0.91	0.5	8382	60
williams syndrome association	0.25	0.1	4658	45
williams syndrome famous people	0.11	0.2	2026	89
williams syndrome facial features	1.72	1	1923	31
williams syndrome eyes	0.56	0.9	4975	27
williams syndrome icd 10	0.2	0.3	6200	34
williams syndrome life expectancy	0.61	0.6	8242	2
williams syndrome chromosome	2	0.8	1086	87
williams syndrome convention 2024	1.6	1	1119	24
williams syndrome baby	1.3	0.6	5631	73
williams syndrome convention 2023	0.42	0.7	9386	32
williams syndrome pictures	0.4	1	4551	95
williams syndrome genereviews	1.43	0.4	7580	25
williams syndrome symbol	0.89	0.4	8920	60
williams syndrome personality	1.14	0.1	6093	2
williams syndrome treatment	0.66	0.8	9392	67
williams syndrome nhs	1.23	0.2	2347	17
williams syndrome genetics	1.23	0.6	4310	71
williams syndrome radiology	0.95	0.4	240	43
williams syndrome characteristics	0.02	0.9	9645	32
williams syndrome vs down syndrome	1.16	0.3	9518	24
williams syndrome diagnosis	0.8	0.8	7529	36
williams syndrome conference	0.34	0.1	6025	90

Search Results related to williams syndrome on Search Engine

Williams syndrome - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Williams_syndrome

WEBWilliams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks.

DA: 45 PA: 43 MOZ Rank: 22

Williams Syndrome, Williams Beuren Syndrome: Causes, …
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/15174-williams-syndrome

WEBDec 10, 2021 · Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms including unique physical features, delayed development, cognitive challenges and cardiovascular abnormalities. Williams syndrome may cause poor growth in childhood, and most adults …

DA: 13 PA: 81 MOZ Rank: 29

What is Williams syndrome? | Williams Syndrome Association
williams-syndrome.org

https://www.williams-syndrome.org/what-is-ws

WEBWilliams syndrome (WS) is a genetic condition that is present at birth and can affect anyone. It is characterized by medical problems, including cardiovascular disease, developmental delays, and learning challenges. These often occur side by side with striking verbal abilities, highly social personalities, and an affinity for music.

DA: 28 PA: 52 MOZ Rank: 42

Williams Syndrome: Causes, Symptoms, and Diagnosis - WebMD
webmd.com

https://www.webmd.com/children/williams-syndrome

WEBAug 3, 2022 · Williams syndrome is a rare genetic disorder that causes a variety of symptoms and learning issues. Children with this syndrome could have problems with their heart, blood vessels, kidneys, and...

DA: 45 PA: 58 MOZ Rank: 93

Williams syndrome: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/williams-syndrome/

WEBWilliams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems.

DA: 17 PA: 50 MOZ Rank: 51

Williams Syndrome - National Institute of Neurological Disorders and Stroke
nih.gov

https://www.ninds.nih.gov/health-information/disorders/williams-syndrome

WEBNov 28, 2023 · Williams syndrome (WS) is a rare genetic disorder. People with WS may have mild to moderate delays in their cognitive development (ability to think and reason) or learning difficulties. They also may have a distinctive facial appearance, and a unique personality that combines over-friendliness and high levels of empathy with anxiety.

DA: 56 PA: 26 MOZ Rank: 69

Williams Syndrome: Symptoms, Diagnosis, and Treatments - Healthline
healthline.com

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

WEBJul 9, 2017 · Williams syndrome is a condition made up of specific symptoms that significantly impact health and development. Common symptoms of the condition include: specific facial features like a wide...

DA: 56 PA: 72 MOZ Rank: 72

Williams Syndrome - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK544278/

WEBNov 7, 2019 · Williams syndrome (WS) is a rare genetic and neurodevelopmental disorder. WS often presents at birth when the child is discovered to have supra-vascular aortic stenosis. The child also shows distinctive facies (elfin-like features), hypercalcemia, connective tissue abnormalities, growth abnormalities, intellectual disability, behavior …

DA: 33 PA: 74 MOZ Rank: 38

Williams Syndrome | Boston Children's Hospital
childrenshospital.org

https://www.childrenshospital.org/conditions/williams-syndrome

WEBWilliams syndrome is a rare (affecting 1 in 10,000 people) developmental disorder that can affect many parts of the body, including the heart and blood vessels. Children with Williams syndrome have mild to moderate intellectual disability, distinctive facial features, and an outgoing personality.

DA: 25 PA: 20 MOZ Rank: 47

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

https://www.mountsinai.org/health-library/diseases-conditions/williams-syndrome

WEBWilliams syndrome is a rare disorder that can lead to problems with development. Causes. Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. In most cases, the gene changes (mutations) occur on their own, either in the sperm or egg that a baby develops from.

DA: 7 PA: 38 MOZ Rank: 77