The person appears to be a/an Indian Female, approximately 30 to 39 years old.
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.
Cystic Fibrosis is a genetic disorder that primarily impacts the lungs and digestive system, and it can be particularly challenging for teenagers. It occurs due to a faulty gene that disrupts the balance of salt and water in the body, leading to the production of thick, sticky mucus. This mucus can obstruct the airways, making it hard to breathe and increasing the risk of lung infections, which can be especially concerning for active young individuals. Common symptoms include a persistent cough with mucus, shortness of breath, poor growth, frequent lung infections, fatigue, and digestive problems like constipation and difficulty gaining weight. Early diagnosis and treatment are crucial to manage the condition and improve quality of life.