What do babies with Noonan syndrome look like?

Most children with Noonan syndrome have differences in the shape of their face and head. These are noticeable at birth and include: wide-set pale blue or blue-green eyes. thick, low-set ears.

Can you tell if a baby has Noonan syndrome?

The condition is present from before birth, although milder cases may not be diagnosed until a child gets older. The most common features of Noonan syndrome are: unusual facial features, such as a broad forehead, drooping eyelids and a wider-than-usual distance between the eyes. short stature (restricted growth)

What does someone with Noonan syndrome look like?

Teeth may be crooked, the inside roof of the mouth (palate) may be highly arched and the lower jaw may be small. Facial features may appear coarse, but appear sharper with age. The face may appear droopy and expressionless. Head may appear large with a prominent forehead and a low hairline on the back of the head.

When babies eyes are far apart?

Hypertelorism is an increase in the distance between the bony orbits, in which the eyes lie. It can be due to a variety of causes. During development as an embryo, the eyes lie widely apart and gradually move closer together.

Is Noonan syndrome like autism?

Few reports have described the psychiatric co-morbidity of Noonan syndrome. While mental retardation is a common feature of Noonan syndrome, the diagnosis of autism using operational criteria has not been reported. In this paper, the authors describe the association of Noonan syndrome with autism.

Overcoming Noonan Syndrome Through Therapy

Can Noonan syndrome go undiagnosed?

The condition is usually diagnosed at birth, although milder cases may go undiagnosed until a child gets older. Noonan syndrome is relatively uncommon.

What do wide set eyes indicate?

In orbital hypertelorism, the eye sockets fail to rotate into their normal position, resulting in wide-set eyes with extra bone between the eyes.

Is it normal for baby to have short neck?

Yes ... it's there. Normally the neck looks short in newborns because it tends to get lost in the chubby cheeks and folds of skin.

What is a Michelin baby?

Michelin tire baby syndrome (MTBS) is a benign hamartomatous condition with ring-like lesions present on the limbs and trunk. MTBS is a rare genodermatosis.

Can Noonan syndrome be cured?

There's no cure for Noonan syndrome, but medical care can help with almost every symptom. For example: Medicines and surgery can help heart problems. Medicines or blood transfusions can treat bleeding.

Does Noonan syndrome affect behavior?

behavioural problems – some children with Noonan syndrome may be fussy eaters, behave immaturely compared to children of a similar age, have problems with attention and have difficulty recognising or describing their or other people's emotions.

Is Noonan syndrome more common in males or females?

Affected Populations

Noonan syndrome appears to affect more males than females and is thought to affect approximately one in 1,000 to one in 2,500 people.

Is Noonan syndrome a disability?

The majority of children who are diagnosed with Noonan syndrome have average intelligence, although a small percentage have special educational needs, and some experience intellectual disability.

What does Waardenburg syndrome look like?

The most common symptoms of Waardenburg syndrome are pale skin and pale eyes. Another common symptom is a streak of white hair near the forehead. In many cases, someone with this condition might have two different-colored eyes.

What is mild Noonan syndrome?

Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.

How long is the average lifespan of a person with Noonan syndrome?

It is one of the most common non-chromosomal disorders in children with congenital heart disease, with an estimated prevalence worldwide of 1 in 1000-2500. The average age at diagnosis is nine years, and life expectancy is likely normal if serious cardiac defects are absent.

What is the survival rate of Noonan syndrome?

Summary: Infants less than six months old with Noonan Syndrome, hypertrophic cardiomyopathy and congestive heart failure normally have a poor prognosis, with a one-year survival rate of 34 percent.

Does Noonan syndrome have mental retardation?

The cardinal features of Noonan syndrome include unusual facies (ie, hypertelorism, down-slanting eyes, webbed neck), congenital heart disease, short stature, and chest deformity. Approximately 25% of individuals with Noonan syndrome have mental retardation.

What syndrome causes wide set eyes?

Type 1. Type 1 Waardenburg syndrome causes someone to have a wide space between their eyes.

What is the long term outlook for a child with Noonan syndrome?

Some affected children may also have other ongoing health problems such as problems urinating, blood disorders, etc. However, with special care and counselling, the majority of children with NS grow up and function normally as adults. The long-term prognosis of people with Noonan syndrome is variable.

Is Noonan syndrome life threatening?

Some patients with mild symptoms and signs will have a normal life expectancy, while others with severe symptoms and signs may have a shortened lifespan. The highest risk of death is in young adults who have hypertrophic cardiomyopathy that was diagnosed when they were under 2 years old.

What causes Noonan's disease?

Noonan syndrome is caused by a faulty gene, which is usually inherited from one of the child's parents. There's no evidence to suggest the genetic fault is caused by environmental factors, such as diet or exposure to radiation.

How do I know if my baby has a short neck?

A short neck, which can cause a small difference of appearance between the left and right sides of your face. A low hairline at the back of your head. Limited ability to bend and twist your neck.

What does it mean when a baby has low set ears?

Low-set ears and pinna abnormalities refer to an abnormal shape or position of the outer ear (pinna or auricle). Low set ears (pinna), abnormal rotation, the absence of ears, and abnormal folds in the ear may be associated with various medical conditions.

Does my baby have a syndrome?

Diagnosing Down syndrome

Parents who think their child may have Down syndrome may notice the slanting eyes, flat-appearing face, or low muscle tone. Babies with Down syndrome may seem floppy in activity, and they may take longer to hit developmental milestones. These can include sitting up, crawling, or walking.