Pediatric Pitt-Hopkins Syndrome

Pitt-Hopkins syndrome (PTHS) is an autism spectrum disorder that causes developmental delays. Children’s Health is among a handful of centers in the world with neurodevelopmental disability specialists experienced in diagnosing and treating PTHS.

Only around 500 people worldwide are known to have PTHS. Genetic testing for this condition is relatively new, so more people likely have it but haven’t been tested or formally diagnosed. For a disorder this rare, it’s important to seek care from experienced specialists.

What causes Pediatric Pitt-Hopkins Syndrome?

A mutation (change) in the TCF4 gene causes PTHS. This gene is critical to brain and nervous system development. Some children are missing the part of the chromosome (a tiny structure inside the body that carries DNA) that contains the TCF4 gene.

Experts don’t know why these chromosomal changes happen or why some children get PTHS.

Pediatric Pitt-Hopkins Syndrome Doctors and Providers

Specialists from a variety of fields work together to help families manage PTHS.

Frequently Asked Questions

  • How common is Pitt-Hopkins syndrome?

    Doctors have only known about PTHS since 1978. And the gene change that causes it was just identified in 2007. PTHS may affect as many as 1 in 34,000 to 41,000 people. The numbers are most likely higher because genetic testing for the disorder is fairly new. Some people with mild symptoms don’t know they have it.

  • Is Pitt-Hopkins syndrome inherited?

    PTHS is rarely inherited (passed down from parent to child through genes). Most commonly, it’s the result of a spontaneous, or unexplained, genetic change. If you have PTHS or the gene mutation that causes it, you have a one-in-two chance of passing it to your child. In about 1% to 2% of cases, more than one child in a family has PTHS.

  • Does Pitt-Hopkins syndrome affect more boys than girls?

    PTHS affects boys and girls equally.