This article on Epainassist.com has been reviewed by a medical professional, as well as checked for facts, to assure the readers the best possible accuracy.

We follow a strict editorial policy and we have a zero-tolerance policy regarding any level of plagiarism. Our articles are resourced from reputable online pages. This article may contains scientific references. The numbers in the parentheses (1, 2, 3) are clickable links to peer-reviewed scientific papers.

The feedback link “Was this Article Helpful” on this page can be used to report content that is not accurate, up-to-date or questionable in any manner.

This article does not provide medical advice.


How Long Will It Take To Recover From Noonan Syndrome & How Long Does The Symptoms Last?

Noonan Syndrome (NS) is the most common syndrome that can either be inherited or caused by mutations. It is an autosomal dominant congenital disorder and is named after Jacqueline Noonan, a pediatric cardiologist. According to the National Organization for Rare Disorders, Noonan syndrome is believed to influence roughly 1 in 1,000 to 1 in 2,500 individuals.

The average age at identification is nine years, and life expectancy is probably usual if life-threatening cardiac deficiencies are not present.

How Long Will It Take To Recover From Noonan Syndrome?

While there’s no means to restore the gene variations that trigger Noonan syndrome, therapies can enhance lessen its effects and medical care can help with almost every symptom. The faster a diagnosis is made, and therapy is started, the faster the recovery. However, the treatment is invariably dependent on its type and severity of the condition.

For instance, Medications and surgical procedures can help heart complications. Drugs or blood transfusions can cure bleeding.

Similarly, when the fetus is suspected to have Noonan syndrome during pregnancy, your GP may recommend for pregnancy ultrasound. This test will show the following

  • Excess amniotic fluid in the amniotic sac
  • Cysts all around the fetus neck
  • Cardiac irregularities

When the baby shows any of the above-mentioned symptoms, the doctor will prescribe for possible treatments to treat the complications. For example, your doctor will recommend for growth hormones for developmental delays.

As Noonan syndrome stems from a genetic defect, there is no complete recovery. Therefore, Noonan syndrome patients must live with this condition. To be more concise, there is no defined timeline for the recovery of this disorder.(2,3)

How Long Does The Noonan Syndrome Symptoms Last?

A medical survey was conducted by the National Center for Advancing Translational Sciences among Noonan syndrome patients. The survey showed that people with Noonan syndrome have a threefold greater death rate than the overall population.

Besides, the symptoms vary between persons therefore, the symptoms last depending on the severity of the disorder. Long-term diagnosis is likely to depend on the existence and seriousness of heart faults. Death in affected patients has been often related to the incidence of complicated left ventricular infection.

However, conditions that were identified and treated early, showed more proper management of the symptoms and these patients were able to lead independent lives in their adulthood.

The medical complications of Noonan syndrome can be traumatic for your child and you. But you’re not alone.

The scientists look for better ways to prevent and treat Noonan syndrome. You can also ask about support groups to help cope with challenges and to assist your loved ones.(4,5)

Noonan syndrome is a genetic condition that affects various functionalities of the body. Patients diagnosed with this condition are known to suffer frequent cardiac ailments such as irregular heart rhythms and thickening of the heart muscle, and they may also experience developmental delays. Due to advance development in clinical studies, laboratory experiments are available to diagnose this condition.

In general, Noonan syndrome is diagnosed through prenatal testing and blood tests. The symptoms of this disorder are very subtle, therefore in many cases, the symptoms are not identified until adulthood. Treatment for the condition is tailored to the specific needs of each patient. Some conditions are treated through therapies and in some cases, patients may require surgery to improve symptoms and to manage conditions. Some of the potential complications include

  • Excessive bleeding and bruising
  • High risk of cancer
  • Developmental delays
  • Complications with the lymphatic systems
  • Urinary tract infections and a few others.(1)


  1. Noonan Syndrome – Cincinnati Children’s Hospital https://kidshealth.org/en/parents/noonan-syndrome.html
  2. Noonan syndrome – Treatment – NHS https://www.nhs.uk/conditions/noonan-syndrome/treatment/
  3. What Is Noonan Syndrome? Does My Child Have the Signs? https://www.webmd.com/children/noonan-syndrome#1
  4. Noonan syndrome | Genetic and Rare Diseases Information https://rarediseases.info.nih.gov/diseases/10955/noonan-syndrome
  5. Noonan Syndrome – American Family Physician https://www.aafp.org/afp/2014/0101/p37.html

Also Read:

Pramod Kerkar, M.D., FFARCSI, DA
Pramod Kerkar, M.D., FFARCSI, DA
Written, Edited or Reviewed By: Pramod Kerkar, M.D., FFARCSI, DA Pain Assist Inc. This article does not provide medical advice. See disclaimer
Last Modified On:December 17, 2019

Recent Posts

Related Posts