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 ...
May 25, 2023 · This genetic condition stops typical development in parts of the body. It may include unusual facial features, short height, heart problems ...
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