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 move in and out of cells. 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 be very serious.
Cystic Fibrosis is a hereditary genetic disorder that primarily impacts the respiratory and digestive systems. It arises from a mutation in the CFTR gene, which disrupts the normal balance of salt and water in the body. This leads to the production of thick, sticky mucus that can obstruct the airways, making individuals more susceptible to lung infections and severe respiratory complications. Common symptoms include persistent coughing with mucus, shortness of breath, stunted growth in children, frequent lung infections, fatigue, and gastrointestinal issues such as constipation and difficulty in gaining weight. Early diagnosis and management are crucial, as untreated Cystic Fibrosis can significantly reduce life expectancy.