Tetrasomy 18p

Tetrasomy 18p is a genetic condition where an individual has an extra chromosome made up of two copies of the short arm of chromosome 18, resulting in four total copies. This condition can lead to various medical and developmental issues, although the severity and symptoms vary among individuals. Common concerns include developmental delays, heart defects, spina bifida, and other health issues. Diagnosed usually through blood tests in infants or children with health concerns, Tetrasomy 18p requires ongoing medical care and support.

For a more comprehensive understanding of Tetrasomy 18p, please refer to the detailed information provided in the Tetrasomy 18p (English) or Tetrasomy 18p (Spanish) handouts that are downloadable and printable items.