Noonan syndrome is a genetic condition that can ... and some patients may need to have an ultrasound or CT or MRI scans. A cystoscopy is sometimes recommended to allow the doctor to examine ...

Noonan syndrome is a rare genetic disorder. If you have it, you might have certain identifiable facial features, short height, and unusual chest shape. You may also have heart defects. It can ...

Cerebral MRI showed moderate ventriculomegaly ... MGCL with an NS phenotype was an independent NL entity, the NL/MGCL syndrome. The mutations observed in patients with MGCL are not different ...

Noonan syndrome is a genetic disorder that affects one in 2,000 children. It is characterized by unusual facial characteristics, cardiac abnormalities, short stature, anomalies of certain blood ...

Noonan syndrome is a genetic disorder that prevents normal development in the body. A person can be affected by Noonan syndrome in various ways such as with unusual facial characteristics ...

Noonan syndrome is a relatively common genetic disorder characterized by short stature, unique facial features, and heart defects. About 10-15 percent of affected individuals have mutations in ...

Worried, her parents took her to the emergency room. There doctors discovered that Maria, who at age 2 was diagnosed with Noonan syndrome, a genetic disorder that can lead to several health issues ...

Researchers from Loughborough University spoke to 67 families living with Noonan syndrome. The genetic condition affects between one in 2,000 and one in 2,500 UK births, says the NHS. The research ...

Published in the online edition of Nature Neuroscience, the findings were studied in mice genetically engineered to develop the disease, called Noonan syndrome. The disorder can disrupt a child ...