13q deletion syndrome

13q deletion syndrome is a genetic condition caused by the loss of a small piece of chromosome 13. This missing genetic material can lead to a range of health issues, including intellectual challenges, developmental delays, and physical differences such as eye or ear abnormalities and heart defects. The severity varies depending on how much of the chromosome is deleted. Some individuals may have mild symptoms, while others experience more significant health and developmental challenges. It's a rare condition, and diagnosis often involves genetic testing. Management typically includes specialized medical care and developmental support tailored to each person's needs.