Familial Hypercholesterolemia Case: After 40 years old, the danger of heart disease increases, but in very few cases, these diseases can develop at a very young age. Recently, an amazing case has come to an amazing matter from Mumbai’s skills. A 22-year-old woman had severe pain in the chest. The pain was unbearable, and was taken to the doctor. When the doctors examined his ECG, he was amazed at all the heart of the 22-year-old woman. At this age, it is not common, but it was a rare case.
After that, the doctors’ teams took coronary artery bypass surgery, which he became the youngest of the country with the country of surgery. Now, the question is: How at the age of 22, how did the arthritis come into obstructions?
After surgery, the girl’s family said he was experiencing the yellowish knots from the age of 7, after the age of 7. They began at the beginning that it is a skin disease. When he was in 10th grade, a knot was taken with surgery, but the doctors ignore it. As a result, the girl’s condition deteriorated.
The girl’s surgery cardiac surgeon Dr. Amit Karad told toi that Zanthoma is a clear sign of this genetic disorder. It is possible that the doctors who checked her first, they have been misunderstood for simple swelling. His tests revealed serious obstacles in coronary arthritis. It was a rare case while watching his age and gender, as Estrogen provides natural protection against the heart disease.
The girl’s condition was so deteriorating that angeoplasty was not possible. Therefore, doctors decided to take coronary artery bypass surgery. The investigation also came to the same symptoms in his 21-year-sister and 8-year-old brother.
In Mumbai, 79 General doctors in the 2022 survey, only 31% of the doctors identified the Family Hycomolestrolemia. Most were ignorant that one of their patients could be. This disease has no permanent treatment, but it can be controlled with the correct diet and timely investigation. The case highlights the doctors to be aware of the doctors to be aware of the families like family hyacrolemia, so that the symptoms can be identified quickly and the patients are saved.