wiedemann steiner syndrome | Wiedemann-Steiner syndrome

Keyword	CPC	PCC	Volume	Score	Length of keyword
wiedemann steiner syndrome	0.55	0.8	3657	4	26
wiedemann	0.92	0.4	7377	53	9
steiner	0.77	0.7	7031	43	7
syndrome	1.98	0.8	1421	12	8

Keyword	CPC	PCC	Volume	Score
wiedemann steiner syndrome	0.51	0.2	4403	63
wiedemann steiner syndrome icd 10	0.75	0.8	7031	28
wiedemann steiner syndrome genereviews	0.66	0.6	5592	97
wiedemann steiner syndrome symptoms	1.64	0.2	662	87
wiedemann steiner syndrome uk	1.49	0.7	397	100
wiedemann steiner syndrome nhs	0.53	0.3	4029	69
wiedemann-steiner syndrome life expectancy	1.55	0.8	372	85
wiedemann steiner syndrome pictures	1.23	0.7	1826	84
wiedemann steiner syndrome john hopkins	1.29	0.7	3867	36
wiedemann steiner syndrome immunodeficiency	0.4	0.5	9501	69
wiedemann steiner syndrome dental	0.5	0.1	7232	100
wiedemann steiner syndrome behavior	0.86	0.4	5133	49
wiedemann steiner syndrome prognosis	1.97	0.1	6716	61
what is wiedemann steiner syndrome	1.98	0.1	5276	73
syndrome de wiedemann steiner	0.39	0.8	2708	5

Search Results related to wiedemann steiner syndrome on Search Engine

Wiedemann-Steiner syndrome - About the Disease - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/5565/wiedemann-steiner-syndrome/

WEBSummary. Wiedemann-Steiner syndrome (WSS) includes distinctive facial features, growth delay, and intellectual disability. Signs and symptoms vary, but facial features may include thick eyebrows, wide-spaced eyes, and narrow eye openings.

DA: 97 PA: 47 MOZ Rank: 46

What is Wiedemann-Steiner Syndrome? - WSS Foundation
wssfoundation.org

http://www.wssfoundation.org/wiedemann-steiner-syndrome/

WEBWiedemann-Steiner Syndrome (WSS) is a rare genetic disorder resulting from mutations in the MLL (also known as KMT2A) gene on the long arm of chromosome 11. The syndrome was clinically described in 1989, but was not genetically identified until 2012 by a group of researchers in England lead by Dr. Wendy Jones.

DA: 33 PA: 12 MOZ Rank: 55

Wiedemann–Steiner syndrome - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Wiedemann%E2%80%93Steiner_syndrome

WEBWiedemann–Steiner syndrome (WSS) is a rare genetic disorder that causes developmental delay, unusual facial features, short stature, and reduction in muscle tone . The syndrome was originally described in 1989 by Hans-Rudolf Wiedemann. The genetic basis for the syndrome was identified by Dr. Wendy D. Jones in 2012.

DA: 75 PA: 89 MOZ Rank: 99

Wiedemann-Steiner Syndrome - Symptoms, Causes, Treatment
rarediseases.org

https://rarediseases.org/rare-diseases/wiedemann-steiner-syndrome/

WEBJun 29, 2023 · Summary. Wiedemann-Steiner syndrome (WSS) is a rare genetic condition that can affect multiple organ systems. Many patients with this condition have symptoms including developmental delay, intellectual disability or autism and excessive hair growth in unusual places on the body (hypertrichosis).

DA: 92 PA: 88 MOZ Rank: 6

Wiedemann-Steiner Syndrome - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK580718/

WEBMay 26, 2022 · Wiedemann-Steiner syndrome (WSS) is characterized by developmental delay, intellectual disability, and characteristic facial features, with or without additional congenital anomalies. The facial features include thick eyebrows with lateral flare, vertically narrow and downslanted palpebral fissures, widely spaced eyes, long eyelashes, wide ...

DA: 83 PA: 6 MOZ Rank: 50

Wiedemann Steiner Syndrome - Symptoms, Causes, Treatment
rarediseases.org

https://rarediseases.org/gard-rare-disease/wiedemann-steiner-syndrome/

WEBDisease Overview. Wiedemann-Steiner syndrome (WSS) includes distinctive facial features, growth delay, and intellectual disability. Signs and symptoms vary, but facial features may include thick eyebrows, wide-spaced eyes, and narrow eye openings. People with WSS may also have excessive hair on the elbows, arms, and back; difficulty feeding ...

DA: 37 PA: 68 MOZ Rank: 74

About Wiedemann Steiner Syndrome
wiedemannsteiner.com

http://wiedemannsteiner.com/about-wss/

WEBWiedemann-Steiner syndrome is a rare genetic disorder which can cause developmental delay, feeding challenges, short stature, and low muscle tone. It is inherited in an autosomal dominant fashion, which means that typically neither the mother nor the father will carry the syndrome in their genes.

DA: 50 PA: 97 MOZ Rank: 11

About: Wiedemann-Steiner syndrome - North Carolina State …
ncsu.edu

https://rarediseases.oscar.ncsu.edu/disease/wiedemann-steiner-syndrome/about/

WEBWiedemann-Steiner syndrome is a rare, genetic multiple congenital anomalies/dysmorphic syndrome characterized by short stature, hypertrichosis cubiti, facial dysmorphism (hypertelorism, long eyelashes, thick eyebrows, downslanted, vertically narrow, long palpebral fissures, wide nasal bridge, broad nasal tip, long philtrum), …

DA: 57 PA: 63 MOZ Rank: 55

Wiedemann-Steiner Syndrome (WSS) Foundation
wssfoundation.org

http://www.wssfoundation.org/

WEBAccess the latest data reports on common symptoms, development milestones, and other shared characteristics of WSS. The Wiedemann-Steiner Syndrome Foundation provides education, fosters community, and stimulates research to improve the lives of everyone impacted by WSS.

DA: 71 PA: 76 MOZ Rank: 60

Wiedemann-Steiner Syndrome - MediFind
medifind.com

https://www.medifind.com/conditions/wiedemann-steiner-syndrome/5512

WEBMay 2, 2022 · What is the definition of Wiedemann-Steiner Syndrome? Wiedemann-Steiner syndrome (WSS) includes distinctive facial features, growth delay, and intellectual disability. Signs and symptoms vary, but facial features may include thick eyebrows, wide-spaced eyes, and narrow eye openings.

DA: 71 PA: 58 MOZ Rank: 17