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

Content Provider	Europe PMC
Author	Justin, V. G. Venkatesh, T.
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.
Related Links	https://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC3453954&blobtype=pdf
ISSN	09701915
Volume Number	15
PubMed Central reference number	PMC3453954
Issue Number	2
PubMed reference number	23105261
Journal	Indian Journal of Clinical Biochemistry [Indian J Clin Biochem]
e-ISSN	09740422
DOI	10.1007/bf02883748
Language	English
Publisher	Springer India
Publisher Date	2000-07-01
Publisher Place	New Delhi
Access Restriction	Open
Rights License	© Association of Clinical Biochemists of India 2000
Subject Keyword	Alpha-1-antitrypsin deficiency Serum protein electrophoresis
Content Type	Text
Resource Type	Article
Subject	Clinical Biochemistry

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