The person appears to be a/an Indian Female, approximately 10 to 19 years old.
Cystic Fibrosis is a genetic condition that primarily impacts the lungs and digestive system. It occurs due to a mutation in a gene that affects how salt and water are transported in the body. This leads to the production of thick, sticky mucus that can obstruct the airways, making it easier for infections to develop and causing significant lung damage over time. Common symptoms include persistent coughing with mucus, shortness of breath, slow growth in children, frequent lung infections, fatigue, and digestive problems like constipation and difficulty in gaining weight. Early diagnosis and treatment are crucial to manage the condition effectively and improve quality of life.
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.