ALPHA-1-ANTITRYPSIN DEFICIENCY IN CHILDREN
https://doi.org/10.21518/2079-701X-2017-9-166-170
Abstract
Hereditary deficiency of the alpha-1-antitrypsin occupies a leading position among the causes of chronic nonspecific lung diseases with emphysema formation. Deficiency of alpha-1-antitrypsin is a potentially fatal hereditary disease, under-diagnosed by physicians of various specialities. The authors familiarize pediatricians with this hereditary disease, difficulties of its diagnosis and treatment. There are presented own author`s data on the diagnosis and the experience of the enzyme replacement therapy of alpha-1-antitrypsin deficiency with the drug INN «Alpha-1 antitrypsin human» (Respikam).
About the Authors
S. I. MELNIKRussian Federation
M. V. PINEVSKAYA
Russian Federation
E. A. ORLOVA
Russian Federation
PhD in medicine
S. V. STAREVSKAYA
Russian Federation
PhD in medicine
I. Y. MELNIKOVA
Russian Federation
MD, Prof.
V. I. LARIONOVA
Russian Federation
MD
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Review
For citations:
MELNIK SI, PINEVSKAYA MV, ORLOVA EA, STAREVSKAYA SV, MELNIKOVA IY, LARIONOVA VI. ALPHA-1-ANTITRYPSIN DEFICIENCY IN CHILDREN. Meditsinskiy sovet = Medical Council. 2017;(9):166-170. (In Russ.) https://doi.org/10.21518/2079-701X-2017-9-166-170