Noonan syndrome is a genetic disorder that prevents normal development in various parts of the body. The problem that is most common is fluid that is excessive on the top of the feet or the back of the hands.Most individuals particular males with this syndrome have problems with genitals as well as kidneys.These are varied and include the texture or color of the skin. Surgery can be necessary if there is valve involvement.The child’s height needs to be checked 3 times each year until they are 3 years old and then once each year until adulthood.

See more ideas about Noonan syndrome, Noonan, Syndrome. If you suspect you or your child may have the disorder, see your primary care doctor or your child's pediatrician. Growth hormone may be used to treat short stature in some people with Noonan syndrome.Signs and symptoms of Noonan syndrome vary greatly among individuals and may be mild to severe. Intelligence in the syndrome is often normal.

Features of the face become sharper as well as the eyes become less perceptible. Additionally, occurrence of mental deficit in 25% of individuals will affect any long term prognosis.Life expectancy depends on the complications involved during the life of an individual with this syndrome as well as the severity of those complications.
There can be problems with the muscles of the eye, refractive problems, movement of the eyes that is rapid and problems with the eye nerves.Individuals with this syndrome have a history of bleeding or bruising that is abnormal.This system drains fluid that is excess from the body and aids in fighting infection. Noonan syndrome can cause a variety of other signs and symptoms. Feb 21, 2015 - Explore Adrienne Lehtinen's board "Noonan Syndrome", followed by 118 people on Pinterest. Noonan syndrome is a genetic disorder that causes heart defects, bleeding problems, distinct facial features, and more. Noonan Syndrome - Symptoms, Treatment, Prognosis, Life Expectancy, Pictures and Images.

Individuals who have a severe type of this condition can have a life span that is greatly shorter than those with minor problems.
Some forms of congenital heart disease associated with this disorder include:Noonan syndrome can affect normal growth. Ask the physician about infant stimulation programs.The child will need regular exams every 2 years. Some heart problems can occur later in life. A person with an autosomal dominant disorder — in this case, the father — has a 50% chance of having an affected child with one mutated gene (dominant gene) and a 50% chance of having an unaffected child with two normal genes (recessive genes).Noonan syndrome is caused by a genetic mutation. Any use of this site constitutes your agreement to the Terms and Conditions and Privacy Policy linked below. These mutations can occur in multiple genes. These appearances or signs alter with age:When the baby is younger than one month old, it can have eyes that are down-slanting and wide set, ears that are low-set, groove that is deep and peaks that are wide in the upper lip, neck that is short as well as a hairline that is low in the back.The baby can have eyes that are prominent that slant downward as well as lids that are thickened and a nose depressed at the top with a base that is wide and a tip that is bulbous.The face is usually wide at the forehead and tapers to a chin that is pointed.

Some affected individuals have vision or hearing problems.

Autosomal dominant inheritance pattern Because these genes play a role in the formation of many tissues throughout the body, this constant activation of proteins disrupts the normal process of cell growth and division.A parent with Noonan syndrome has a 50 percent chance (one chance in two) of passing the defective gene on to his or her child. This is the most common problem with the heart seen with this syndrome.Abnormal thickening or growth of the heart muscle – affects 20% of those with Noonan syndrome.Individuals with this syndrome frequently have structural problems of the heart. Pediatric cardiologists are normally the first physicians to see those with Noonan syndrome.