Pediatric Poland Syndrome (Poland Sequence)

Poland syndrome is a condition that is present at birth where there is a problem with muscle development that affects one side of a child’s body.

What is Pediatric Poland Syndrome (Poland Sequence)?

Poland syndrome – also known as Poland sequence – is a congenital (present at birth) disorder. The main characteristic of Poland syndrome are underdeveloped muscles on one side of the body, which results in problems with the chest, shoulder, arm or hand on that side of the body.

Signs and symptoms of Poland syndrome – as well as the severity of the condition – vary from person-to-person, even within the same family. Though the condition usually appears sporadically and is not passed down in families, sometimes multiple members of the same family have the disorder.

What are the causes of Pediatric Poland Syndrome (Poland Sequence)?

The cause of Poland syndrome is not fully understood, but many experts believe that it may be due to a disruption of blood flow during about the sixth week of fetal development.

How is Pediatric Poland Syndrome (Poland Sequence) treated?

Especially in treating children with Poland Syndrome, it is important to personalize treatment to take into account not only the extent of the condition and how the individual patient is affected, but also to look ahead to how that child will grow and develop over time. We offer a wide variety of treatment options for Poland Syndrome. Often the best option for patients is not to treat this condition with surgery.

Pediatric Poland Syndrome (Poland Sequence) Doctors and Providers