Provides information for persons with Noonan syndrome, their families and interested others.

Noonan syndrome is heterogeneous, comprising more than one similar condition of differing cause, some not inherited.

Noonan syndrome, a disorder which is often confused with Turner syndrome because of several physical features that they have in common.

When present at birth, it can be an indication of Turner syndrome or Noonan syndrome.

A study also showed that there is also an increased risk of atrioventricular canal in patients who suffer from Noonan syndrome.

Low levels of factor XI also occur in many other disease states, including Noonan syndrome.

Despite identification of six causative genes, the diagnosis of Noonan syndrome is still based on clinical features.

In the future, there will be scope for targeted management of Noonan Syndrome, depending on what genetic mutation the patient has.

Additionally, it can be associated with Turner syndrome or with Noonan syndrome.

Noonan syndrome.

It was later determined that the child suffered from a pre-existing heart condition that is associated with Noonan Syndrome.

Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia.

Recent studies also show that mutations in Sos1 can cause Noonan syndrome and hereditary gingival fibromatosis type 1.

She presented her first paper on the subject in 1963, and after several more papers and recognition, the condition was officially named Noonan syndrome in 1971.

Growing up in Millburn in the 1960's with a disability called Noonan syndrome wasn't easy for Lee Day.

Among the more common are Down syndrome Prader-Willi syndrome, and Noonan syndrome.

Noonan syndrome (particularly JMML development).

PTPN11: protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1)

Many people affected by Noonan Syndrome suffer from joint pain or muscle pain, particularly in adulthood, which varies in severity.

Having certain genetic disorders, such as Down syndrome, Fanconi anemia, neurofibromatosis type 1, or Noonan syndrome.

The mutations that cause Noonan syndrome thus appear to perturb intramolecular interactions necessary for SOS1 auto-inhibition.

Mutations that cause Noonan Syndrome have been found in PTPN11 and SOS1.

Dominant mutant alleles of SOS1 have recently been found to cause Noonan syndrome and hereditary gingival fibromatosis type 1.

Dale Akiki was born with Noonan syndrome, a rare genetic disorder which left him with a concave chest, club feet, drooping eyelids and ears.

Jacqueline Anne Noonan is a pediatric cardiologist best known for her characterization of a genetic disorder now called Noonan syndrome.