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α 1-antitrypsin deficiency

　　 α 1-antitrypsin deficiency is an antiprotein component in blood- α 1-antitrypsin α 1-AT) deficiency is a congenital metabolic disease, which is inherited by autosomal. The clinical features are neonatal hepatitis, liver cirrhosis, liver cancer and emphysema in infants and adults.

Symptoms

Coramine poisoning

perforated peptic ulcer

Krigler Nagar syndrome

Ulcer bleeding

Acute perforation of ulcer

Crohn's disease arthritis

Jejunal and ileal diverticulum

Ulcerative colitis arthritis

Quinine poisoning

Ulcer bleeding

Antibiotic toxic nephropathy

Kuru disease

Supraorbital neuralgia

Open brain injury

Post test syndrome

Crabbe's disease

Croytzfeldt Jakob disease

Creutzfeldt Jakob disease dementia

Guest disobedience

Syndrome of abnormal antidiuretic hormone secretion

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