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 ...

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 ...

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 ...

"Mouse model that reproduces noonan syndrome created." ScienceDaily. www.sciencedaily.com / releases / 2014 / 11 / 141105112620.htm (accessed June 2, 2025). Explore More ...

Noonan syndrome is associated with gastrointestinal dysfunction and feeding difficulties in children. We report the case of a 64-year-old man with Noonan syndrome who was admitted to the hospital ...