Alpha-1 Antitrypsin Deficiency and the Hope for a Cure

Have you ever heard about disease, illness, illness? It was only 11 months ago that my baby was diagnosed as alpha - 1 antitrypsin deficiency 11 years ago, but only 4 months after birth. Even if I did not know how it is, what that means, how it changes our lives, my heart fell as they told me to diagnose . I have a lot of problems, and to this day the problem is still infinite. I investigated countless hours and asked questions, which tried to fully understand all the meanings.

K. alpha-1-antitrypsin deficiency 1. Recognize clinical and histological features of alpha-1-antitrypsin deficiency 2. Plan to evaluate patients suspected of alpha-1-antitrypsin deficiency 3. Understanding α-11-antitrypsin deficiency genotype and phenotypic characteristics 4. Understand clinical outcomes which may be the etiology of α-1-patient 3. Treatment plan for familial intrahepatic cholestatic depression patients 4. Disease Understanding Prognosis of patients with progressive familial intrahepatic cholestasia 5. Understanding diagnostic criteria for Alagille syndrome 6. Planning of treatment plan for patients with Alagille syndrome 7. Understanding of prognosis in patients with Alagille syndrome 8. Understanding clinical symptoms of liver disease , Diagnostic criteria and prognosis

Tanya discovered that she is alpha 1 antitrypsin deficiency after undergoing multiple examinations with a doctor at the NY-P liver disease and transplant center. Alpha-1 is a hereditary disorder that can cause liver disease or lung disease - we understand that about 15% of adults with this disease develop liver disease. Symptoms of adults include shortness of breath, mild activity, decreased motor ability. This explains why my wife is too tired. First, the nurse explained about liver transplantation and then came to a psychiatrist, he confirms that my wife is a well-behaved candidate who can take medication by taking prescription drugs. did. Then we met a nutritionist and of course the hospital's claimant. At the end of the day was a social worker who was trying to prepare us as part of a liver transplant plant in New York City.

In about 1% of patients with COPD, the disease is caused by hereditary diseases, resulting in low level proteins called alpha-1-antitrypsin. Alpha-1 antitrypsin (AAt) is made in the liver and is secreted into the blood to help protect the lungs. Alpha-1-antitrypsin deficiency affects the liver and lungs. Infants and children may suffer from lung damage as well as adults with a long history of smoking. Exposing to cigarette smoke. The most important risk factor for COPD is long-term smoking. The older you smoke, the more you pack up you and the greater the risk. Pipeline smokers, cigar smokers, and smokers of marijuana, as well as those exposed to large amounts of secondhand smoke, may also be at risk.