What is Noonan syndrome? Noonan syndrome is a genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems and skeletal abnormalities. Most individuals with Noonan syndrome have normal intelligence, but some may have special educational needs or intellectual disability.
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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 (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and ...
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 is a condition that some babies are born with. It causes changes in the face and chest, and usually includes heart problems.
Jan 9, 2023 · Noonan syndrome is a genetically inherited disease with heterogeneous, phenotypic manifestations. Gene mutations involve the RAAS/MAPK ...
Apr 22, 2022 · Noonan syndrome is a genetic disorder that prevents normal development of various parts of the body. The cardinal features of Noonan ...
A rare, highly variable, multisystemic disorder mainly characterized by short stature, distinctive facial features, congenital heart defects, cardiomyopathy and ...
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.
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