Copertina di Alpha 1-antitrypsin deficiency
Titolo del libro:

Alpha 1-antitrypsin deficiency

Alphascript Publishing (26.07.2010 )

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ISBN-13:

978-613-0-86339-5

ISBN-10:
613086339X
EAN:
9786130863395
Lingua del libro:
Inglese
Risvolto di copertina:
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Alpha 1-antitrypsin deficiency is an autosomal recessive genetic disorder caused by defective production of alpha 1-antitrypsin, leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells. There are several forms and degrees of deficiency. Severe A1A deficiency causes panacinar emphysema and/or COPD in adult life in many people with the condition, as well as various liver diseases in a minority of children and adults, and occasionally more unusual problems. It is treated by avoidance of damaging inhalants, by intravenous infusions of the A1AT protein, by transplantation of the liver or lungs, and by a variety of other measures, but it usually produces some degree of disability and reduced life expectancy.
Casa editrice:
Alphascript Publishing
Sito Web:
https://www.alphascript-publishing.com/
A cura di:
Frederic P. Miller, Agnes F. Vandome, John McBrewster
Numero di pagine:
132
Pubblicato il:
26.07.2010
Giacenza di magazzino:
Disponibile
categoria:
Genetica
Prezzo:
45,00 €
Parole chiave:
Autosomal, Recessive, Genetic, Disorder, blood

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