Find all needed information about Williams Syndrome Parent Support. Below you can see links where you can find everything you want to know about Williams Syndrome Parent Support.
https://williams-syndrome.org/parent
570 Kirts Blvd. Suite 223. Troy, MI 48084-4153 [email protected] 248.244.2229 800.806.1871
https://www.care.com/c/for/williamssyndrome
Why you should join When you’re the parent of a child with Williams syndrome, connecting with other parents is an important part of the journey. The Kinsights Williams syndrome group is a safe and secure online community to get answers from parents, mentors, and experts on Williams syndrome and ...
http://williams-syndrome.org/
Held Biennially, our National Conventions (next in Phoenix in 2020) and International Professional Conferences bring together the foremost experts on Williams syndrome and related characteristics to discuss the latest research findings, medical treatments and educational strategies.
http://williamssyndrome.org.au/
Williams 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 disabilities. It affects 1 in 10,000 people worldwide and occurs equally in …
https://www.dailystrength.org/group/williams-syndrome
Williams Syndrome Support Group. Williams syndrome is a rare genetic disorder characterized by a distinctive, "elfin" facial appearance, an unusually cheerful demeanor, ease with strangers, a love for music, and cardiovascular problems.
https://rarediseases.info.nih.gov/diseases/7891/williams-syndrome
224 rows · Sep 21, 2018 · Williams syndrome is caused by a missing piece (deletion) of genetic …
https://en.wikipedia.org/wiki/William%27s_syndrome
Williams syndrome is a microdeletion syndrome caused by the spontaneous deletion of genetic material from the region q11.23 of one member of the pair of chromosome 7, so that the person is hemizygous for those genes. The deleted region includes more than 25 genes, and researchers believe that being hemizygous for these genes probably contributes to the characteristic features of this syndrome.Complications: Heart problems, periods of high blood …
https://ghr.nlm.nih.gov/condition/williams-syndrome
Oct 29, 2019 · Williams syndrome is considered an autosomal dominant condition because one copy of the altered chromosome 7 in each cell is sufficient to cause the disorder. In a small percentage of cases, people with Williams syndrome inherit the chromosomal deletion from a parent with the condition.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2083767/
Feb 14, 2007 · Individuals were affiliated to the Williams Syndrome Foundation, the UK parent support group (www.williams‐syndrome.org.uk). Written consent was obtained to measure children with Williams syndrome at intervals, obtain blood for chromosome analysis as necessary and review available hospital records. Adults (age >20 years) were measured once.Cited by: 29
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