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Sažetak sa skupa

https://doi.org/10.26800/LV-144-supl2-LR06

SPREADING THE WORD ABOUT ALPHA1-ANTITRYPSIN DEFICIENCY

Andra Diana Tanasa ; University of Medicine and Pharmacy "Gr. T. Popa" Iasi
Adrian Iulian Ababei ; "Alexandru Ioan Cuza" University, Biology


Puni tekst: engleski pdf 757 Kb

str. 93-93

preuzimanja: 108

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Sažetak

Alpha1-antitrypsin is synthesized mainly in the liver and to a lesser degree, by neutrophils and macrophages. Individuals with α1AT deficiency are prone to early onset lung and liver disease. This condition is the most common genetic cause of liver disease in children and an underappreciated cause of liver disease in adults. My aim is to highlight the current knowledge of this condition in hopes of better understanding its role in these diseases and raise awareness regarding the early diagnosis of this deficiency, in order to avoid major deteriorations, misdiagnosis and to ensure an efficient treatment.

Ključne riječi

deficiency, liver, lung

Hrčak ID:

279942

URI

https://hrcak.srce.hr/279942

Datum izdavanja:

27.4.2022.

Posjeta: 388 *