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Indian J Clin Biochem. 2000 Jul;15(2):171-3. doi: 10.1007/BF02883748.

Diagnosis of alpha-1-antitrypsin deficiency by serum protein electrophoresis.

Indian journal of clinical biochemistry : IJCB

V G Justin, T Venkatesh

Affiliations

  1. Department of Biochemistry and Biophysics, St. John's National Academy of Health Sciences, 560034 Bangalore, India.

PMID: 23105261 PMCID: PMC3453954 DOI: 10.1007/BF02883748

Abstract

Alpha-1-antitrypsin deficiency is a hereditary disease leading to hepatitis and cirrhosis. It is the most common genetic cause of liver disease in children which must inherit the tendency from both parents to develop. It acquires the highest priority in the differential diagnosis in a child with chronic liver disease. In this case report we substantiate the role of serum protein electrophoresis, in diagnosing alpha-1-antitrypsin deficiency.

Keywords: Alpha-1-antitrypsin deficiency; Serum protein electrophoresis

References

  1. Pediatrics. 1975 Jul;56(1):91-9 - PubMed
  2. Clin Chem. 1982 Jan;28(1):219-25 - PubMed

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