Kawasaki syndrome symptoms

What are the symptoms of Kawasaki syndrome?

Symptoms and signs develop over the first 10 days, and the disease goes back by itself in most children, even without treatment. Symptoms can vary, but most have:

• Fever for more than five days without explanation
• Conjunctivitis
• Rash - are almost always.
• Lymph node enlargement in the neck - often lack.
• Changes in the oral mucosa
• Changes at the hands and feet
• Lack of effect of antibiotic

A number of other symptoms may also occur in connection with the disease: eg. irritability, joint pain, diarrhea, abdominal pain and ear pain. The changes in the oral cavity consist of redness, cracking and / or crust formation on the lips and strawberry tongue. The changes in hands and feet made of thickened skin, swelling and redness of the palms and soles, desquamation after approx. two weeks.

Symptoms and signs develop over the first 10 days, and the disease goes back by itself in most children, even without treatment.

Kawasaki syndrome causes

What causes Kawasaki Syndrome?
The cause is unknown. Probably, there are a number of factors that contribute to disease, but there are indications that there is an infection.

However, they have not been able to detect any virus or microbe.

In the acute phase developed inflammation of the wall of the coronary arteries (coronary vasculitis).

This can lead to a moderate expansion of the coronary artery.

The lesions may persist from a few weeks to over a year after the disease onset.

What is Kawasaki Syndrome

What is Kawasaki Syndrome?

It is a febrile illness in children with rash, mucosal changes and lymph node enlargement. There is inflammation in the body's blood vessels (vasculitis). The condition is self-limiting and resolves by itself. Although the condition is by itself, one can get without late effects of treatment. The development of ballooning (aneurysm) of a coronary arteries (coronary arteries) in 20-25% if you do not receive treatment. In time, these sinuses interspersed cause serious complications. The disease was first described in Japan in the 1960s.

The disease affects children aged from three months to 12 years, 85% are under five years a . Isolated cases in adults are described. Sweden has found an annual incidence of 6.2 cases per 100,000 under five. The incidence of the disease varies throughout the year, with peaks in winter and spring.

The syndrome is most commonly in Asians, a little less frequently among blacks and lowest among whites. The incidence in the West is increasing.