Kawasaki’s disease is named after Japanese doctor Tomisaku Kawasaki, who first described the condition in 1967. It is the most common non-congenital heart disease in children in developed countries. Nevertheless, the disease is still a rare condition. It is a disease that mainly affects young children: 80 to 90 percent of all cases are detected in children aged 5 years or younger. In this group of young children, the disease is diagnosed annually in 4 to 25 children per 100,000 children. However, the condition is more common in children from East Asian countries. In Japan, for example, the number of cases is up to 20 times higher than in European countries.

What is Kawasaki’s disease?

Kawasaki’s disease is characterized by widespread inflammation of the blood vessels. In particular, the medium-sized blood vessels, such as the arteries that supply the heart with blood, are affected by the disease.

Scientists suspect that a combination of genetic predisposition and infection causes the disease. This has not yet been confirmed in scientific research. Therefore, the cause of the condition remains unknown for the time being.


The most typical symptoms of this condition are:

  • fever, which persists for more than four days and is above 38.5 degrees Celsius or 101.3 Fahrenheit
  • inflammation of the mucous membranes around the mouth. This manifests itself, among other things, in a strawberry tongue and cracks of the lips.
  • irritation and red discoloration of the whites of the eyes
  • swollen lymph nodes in the neck
  • Rashes
  • hardening and flaking of the skin of the hands and feet. This symptom is usually observed only after a week.


Most parents will quickly schedule a doctor’s visit for their child, due to the persistent fever seen in the disease. The doctor will then make the diagnosis based on the above symptoms, where the long-term fever is the main symptom. Additional examination, such as a blood draw or liver function test, is used to confirm the diagnosis.

Course of the disease

Kawasaki’s disease lasts on average six to eight weeks and can be divided into three phases:

  • The acute phase: at this stage, the disease manifests itself in the symptoms described above. Without treatment, this phase can last up to four weeks. With  treatment, this phase is more likely to last one to two weeks.
  • The subacute phase: apart from the changes on the hands and feet, the external symptoms disappear into the background. However, children at this stage have the highest risk of developing a dangerous heart defect. The subacute phase lasts two to three weeks.
  • Recovery phase: the symptoms now disappear in the whole. This phase can last a few weeks and is only over when the child’s blood values are back to normal.

The child is now cured of the disease. However, during the course of the disease, the child may have developed an aneurysm. This is a local dilation of a blood vessel. Up to 25% of patients develop an aneurysm in one of the blood vessels that supply the heart with blood. This is a dangerous heart defect, which can lead to sudden death.


  • Medication

The medical treatment of Kawasaki’s disease is aimed at preventing the development of heart defects and alleviating the symptoms of the disease. A study of Japanese children found that timely treatment with the right medication reduces the risk of an aneurysm in the heart from 20% to 4%. The medicinal treatment is therefore essential to offer the child the best possible future perspective.

  • Lifestyle

Children who have experienced Kawasaki’s disease have an increased risk of cardiovascular disease later in life. Therefore, adjusting the lifestyle is an important means in the treatment of these patients. You can think of a healthy diet, sufficient physical activity, no smoking and avoiding obesity.

In severe cases, surgery can help treat the complications caused by Kawasaki’s disease.

Cassidy Perry

A certified dietician specializing in diabetes care, Cassidy has over a decade of experience working with diverse patient backgrounds. She writes health-related articles for the Scientific Origin.