Noonan Syndrome

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    Related websites

    Noonan syndrome - Symptoms and causes - Mayo Clinic

    May 25, 2023 · noonan syndrome is a genetic condition that stops typical development in various parts of the body. It can affect a person in several ways, including unusual facial features, short height, heart problems and other physical problems.

    Mayoclinic.org


    Noonan syndrome - Wikipedia

    noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. [1] . Facial features include widely spaced eyes, light-colored eyes, low-set ears, a …

    En.m.wikipedia.org


    Noonan Syndrome - StatPearls - NCBI Bookshelf

    Jan 9, 2023 · noonan syndrome is a genetically inherited disease with heterogeneous, phenotypic manifestations. Gene mutations involve the RAAS/MAPK (mitogen-activated protein kinase) signaling pathway. The patient presentation can range from mild to severe.

    Ncbi.nlm.nih.gov


    Noonan syndrome - UpToDate

    Jun 13, 2022 · noonan syndrome (NS) is a common autosomal-dominant condition that is associated with short stature and congenital heart disease (CHD), most often pulmonic stenosis. It is clinically and genetically heterogeneous.

    Uptodate.com


    Noonan syndrome - Diagnosis and treatment - Mayo Clinic

    May 25, 2023 · Although there's no cure for noonan syndrome, treatments can help decrease its effects. The earlier a diagnosis is made and treatment begins, the greater the benefits. Treatment for noonan syndrome depends on the symptoms and complications and how serious they are.

    Mayoclinic.org


    Noonan syndrome - Symptoms, diagnosis and treatment | BMJ

    Oct 14, 2021 · noonan syndrome (NS) is a relatively common, autosomal-dominant inherited disorder that is predominantly characterised by short stature, subtle facial dysmorphisms, chest deformity, congenital heart disease, and variable degrees of developmental delay.

    Bestpractice.bmj.com


    Noonan Syndrome (Leopard Syndrome): Causes & Outlook

    noonan syndrome is a genetic condition that can affect your child in many ways. While some children born with this condition have mild symptoms, others can have more issues. Symptoms typically include unusual facial features such as a tall forehead and wide-set eyes, lower-set ears and a shorter neck.

    My.clevelandclinic.org


    Noonan Syndrome: Symptoms, Diagnosis, Treatment, and More

    Apr 29, 2022 · What is noonan syndrome? noonan syndrome is a congenital disorder, which means it’s present at birth. It may result from any of eight different gene mutations and can be inherited from a

    Healthline.com


    Noonan syndrome - MedlinePlus

    noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.

    Medlineplus.gov


    Noonan Syndrome: What Is It, Causes, Treatment and More

    Feb 28, 2023 · noonan syndrome is a congenital genetic disorder that prevents typical development in many areas of the human body, leading to a wide range of distinctive physical features and health conditions, such as facial characteristics, short stature, heart defects, and developmental delays.

    Osmosis.org


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