What Is Noonan Syndrome? 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.
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Jun 1, 2018 · Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, ...
May 25, 2023 · This genetic condition stops typical development in parts of the body. It may include unusual facial features, short height, heart problems ...
Read about Noonan syndrome, which is a genetic disorder that causes a wide range of features, such as heart abnormalities and unusual facial features.
Noonan syndrome is a genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems, and skeletal ...
Noonan syndrome
Genetic disorder
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Noonan syndrome is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. Facial features include widely spaced eyes, light-colored eyes,... Wikipedia
Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and ...
Jan 9, 2023 · Noonan syndrome is a genetically inherited disease with heterogeneous, phenotypic manifestations. Gene mutations involve the RAAS/MAPK ...
Aug 21, 2019 · In the majority of cases Noonan syndrome is an autosomal dominant genetic disorder caused by abnormalities (mutations) in more than eight genes.
A rare, highly variable, multisystemic disorder mainly characterized by short stature, distinctive facial features, congenital heart defects, cardiomyopathy and ...
Read about the characteristic features of Noonan syndrome, including unusual facial features, short stature and heart defects.
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