Noonan Syndrome Parent Support

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Noonan Syndrome Foundation

    https://www.teamnoonan.org/
    support your foundation How to help The Noonan Syndrome Foundation is an organization that was created to help support, educate, and advocate for and on behalf of all those who have bee affected by Noonan Syndrome.

Noonan syndrome parent support group - Care.com Community

    https://www.care.com/c/for/noonan-syndrome
    Parenting a child with Noonan syndrome comes with many challenges and questions, whether your child had a recent Noonan syndrome diagnosis or has been living with the condition for years. Wherever you are in your journey, we’d like to invite you to join our online support community for parents who have children with NS. In the group you’ll ...

Noonan syndrome - Symptoms and causes - Mayo Clinic

    https://www.mayoclinic.org/diseases-conditions/noonan-syndrome/symptoms-causes/syc-20354422
    Noonan syndrome can develop because of a new mutation in children who don't have a genetic predisposition for the disorder (de novo). Risk factors A parent with Noonan syndrome has a 50 percent chance (one chance in two) of passing the defective gene on to his or her child.

Noonan Syndrome (for Parents) - Nemours KidsHealth

    https://kidshealth.org/en/parents/noonan-syndrome.html
    Noonan syndrome is a condition that some babies are born with. It causes changes in the face and chest, usually includes heart problems, and slightly raises a child's risk of blood cancer (leukemia). Noonan syndrome is a pretty common condition, affecting 1 in 1,000–2,500 babies. The symptoms of ...

Organizations: Are there support groups for Noonan ...

    https://www.thinkgenetic.com/diseases/noonan-syndrome/organizations/59301
    What websites have good information about Noonan syndrome? How do I find other people with Noonan syndrome? Are different features associated with different genes for Noonan syndrome? Where did the name Noonan syndrome come from? What is the testing for Noonan syndrome?

About Noonan Syndrome NHGRI

    https://www.genome.gov/Genetic-Disorders/Noonan-Syndrome
    Dec 23, 2013 · Noonan syndrome is inherited in families in an autosomal dominant pattern. This means that a person who has Noonan syndrome has one copy of an altered gene that causes the disorder. In about one-third to two-thirds of families one of the parents also has Noonan syndrome.

Noonan Syndrome - St. Jude Children’s Research Hospital

    https://www.stjude.org/disease/noonan-syndrome.html
    Some children with Noonan syndrome inherit a gene mutation in PTPN11, SOS1, RAF1, KRAS, NRAS, BRAF and MAP2K1 from a parent who also has the syndrome. Other people with Noonan syndrome have a new gene mutation that did not come from a parent. These children have no history of the syndrome in their families.

Support Noonan Syndrome Awareness Association

    https://noonansyndrome.com.au/support/
    Support We know how troubling, uncertain and fearsome the diagnosis of Noonan Syndrome can be for you or your loved ones. The NSAA wants you to know you're not

Noonan syndrome Genetic and Rare Diseases Information ...

    https://rarediseases.info.nih.gov/diseases/10955/noonan-syndrome
    88 rows · Oct 02, 2017 · Noonan syndrome is a genetic disorder that causes abnormal development …

Resources Noonan Syndrome Awareness Association

    https://noonansyndrome.com.au/resources/
    NSAA Teaching Guide for Noonan Syndrome (PDF version) Click here for resource. Please share this Noonan Syndrome Child Care Fact Sheet with your teachers/educators and daycare professionals: Click here for resource. NSAA Noonan Syndrome Fact Sheet: click here. Practical Guide for Families with Rare Chromosomal Disorders: Click here



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