Brooklyn Maglinger, now 20 years old, started experiencing severe abdominal pain at the age of 15. Despite visiting multiple gastroenterologists and emergency rooms, doctors were unable to determine the cause of her pain. It wasn’t until she underwent genetic testing that they discovered she had a rare genetic disorder known as cystic fibrosis.
Cystic fibrosis is a life-threatening condition that affects the lungs and other organs, causing thick mucus to build up and leading to serious respiratory and digestive complications. Although cystic fibrosis is most commonly diagnosed in early childhood, Maglinger’s case highlights the importance of considering the condition even in cases where symptoms may not present until later in life.
This discovery has had a significant impact on Maglinger’s life, as she now requires daily treatments and medications to manage her symptoms and prevent complications. It also serves as a reminder of the importance of genetic testing in diagnosing rare genetic disorders and providing appropriate treatment.
