Overview. 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.
May 25, 2023
People also ask
What is the Noonan syndrome?
What is the life expectancy of a child with Noonan syndrome?
What is the female version of Noonan syndrome?
What are the cardinal features of Noonan syndrome?
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, ...
Read about Noonan syndrome, which is a genetic disorder that causes a wide range of features, such as heart abnormalities and unusual facial features.
Places
Location unknown
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
>
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 genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems, and skeletal ...
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 ...
A rare, highly variable, multisystemic disorder mainly characterized by short stature, distinctive facial features, congenital heart defects, cardiomyopathy and ...
Apr 22, 2022 · Noonan syndrome is a genetic disorder that prevents normal development of various parts of the body. The cardinal features of Noonan ...
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.
Related searches
Related conditions
For informational purposes only. Consult your local medical authority for advice.
Related symptoms