The person appears to be a/an White Female, approximately 10 to 19 years old.
Cystic Fibrosis is a genetic condition that mainly affects the lungs and digestive system. It happens because of a faulty gene that changes how salt and water are managed in the body. This leads to thick, sticky mucus that can block the airways, making it hard to breathe and causing frequent lung infections. Some common symptoms include a persistent cough with mucus, trouble breathing, slow growth, and digestive problems like constipation and difficulty gaining weight. If not managed properly, it can become very serious.
Cystic Fibrosis is a hereditary genetic disorder primarily affecting the lungs and digestive system. It arises from mutations in the CFTR gene, which disrupts the normal transport of salt and water in cells. This leads to the production of thick, sticky mucus that obstructs airways and promotes chronic lung infections, as well as digestive complications. Common symptoms include persistent coughing with mucus, shortness of breath, stunted growth in children, frequent respiratory infections, fatigue, and gastrointestinal issues like constipation and malnutrition. Early diagnosis and management are crucial, as untreated Cystic Fibrosis can significantly reduce life expectancy.