These are not caused by anything that a parent does or does not do. Because they happen with each pregnancy, it is only important for a person if they happen in a gene that can cause a medical condition. This means that it is a new change in the individual with CS and not inherited. Most of the time, the genetic change is present in the child but not in the parents. However, we do not find a genetic change in all individuals with features of CS. It is caused by a change or variant in at least one gene. What Causes CHARGE Syndrome?ĬS is a genetic condition. Having a good understanding of the issues and the supports for children and families can help children with CS reach their potential and have a great quality of life. The medical challenges for children with CS can seem overwhelming and hard to manage. Vision and hearing difficulties (CS is the leading cause for babies born deaf and blind).Laryngomalacia (underdevelopment of the upper airway causing breathing problems). Many other conditions can be linked with CS such as: Ear and hearing anomalies (thus the acronym CHARGE).Atresia of the nasal choanae (connection between the back of the nose and throat).Colobomas (a hole in the structures of the eye).CS is a very complex syndrome which often involves: It is rare and affects one in each 150,000 births worldwide. CHARGE syndrome (CS) refers to a pattern of birth defects with a wide range of conditions that can differ from child to child.
0 Comments
Leave a Reply. |