Pediatric Amyloidosis

Amyloidosis occurs when amyloid – a protein produced in the bone marrow ­– builds up in organs and tissues, affecting their function.

What is Pediatric Amyloidosis?

Amyloidosis is a rare condition that occurs when the protein amyloid builds up in the heart, kidneys, liver, or other organs or tissues. Normally, amyloid is produced in the bone marrow and deposited into other tissues and organs. When too much amyloid builds up, it causes problems with the way the organs function. Severe amyloidosis can cause organ failure.

What are the different types of Pediatric Amyloidosis?

There are several types of amyloidosis, and depending on the type your child has, different organs and tissues may be affected. Types of amyloidosis include:

AL amyloidosis (immunoglobulin light chain amyloidosis)

AL amyloidosis is the most common form of the condition and was previously called primary amyloidosis. AL amyloidosis happens when the bone marrow produces abnormal antibodies that cannot be broken down by your child’s body and therefore, interfere with normal function. This most often affects the heart, kidneys, skin, nerves and liver.

What are the causes of Pediatric Amyloidosis?

In general, amyloidosis is caused by the buildup of an abnormal protein called amyloid. The specific cause of the condition can vary based on the type of amyloidosis your child has.

Pediatric Amyloidosis Doctors and Providers