Pitt Hopkins Syndrome is a genetic disorder that affects a specific gene in chromosome 18 called TCF4, according to the Pitt Hopkins Research Foundation.

Stacy has Pitt Hopkins syndrome, an extremely rare condition, and breath-holding is one of the main symptoms of the condition. “It took us 10 years to finally […] Skip to content ...

Pitt-Hopkins syndrome is caused by a mutation within a gene on the 18th chromosome. Besides creating problems with walking and speech, ...

Pitt-Hopkins syndrome arises in a child when one copy of the gene TCF4 is missing or mutated, resulting in an insufficient level of TCF4 protein. Typically, ...

UCSF Benioff Children’s Hospital San Francisco has opened the third Pitt Hopkins Syndrome (PTHS) clinic in the world, giving patients with this rare genetic condition access to an interdisciplinary ...

SARATOGA SPRINGS, N.Y. – Sept. 18 was national Pitt-Hopkins Syndrome Awareness Day. Locally, one family is doing all they can to raise awareness and funds for research to fight the genetic di… ...

Pitt-Hopkins syndrome presents with autism-like symptoms and affects intellectual ability, speech and motor skills, causing a range of medical issues and behavioral differences. The disorder is caused ...

Sat, 28 Jun 2025 10:31:36 GMT (1751106696707) Story Infinite Scroll - News3 v1.0.0 (common) eb2cf0f8a70b793da9d10843fac36cb9c0e32262 ...