Alpha-1 antitrypsin, serum

This is an old revision of the document!

Late neonatal intracranial haemorrhage

Alpha-1-antitrypsin (AAT) deficiency is a rare genetic disorder characterized by hepatitis in neonates, childhood and adulthood (protease inhibitor (PI)*ZZ) and emphysema with or without hepatitis (PI*ZZ)/(PI*SS,SZ or null) in adulthood^[1].
AAT deficiency is a rare genetic disorder that can lead to a serious bleeding disorder in the neonatal period if not recognised on time

1. ^a Kats-Ugurlu G, et al. Eur J Pediatr. 2011 Jan;170(1):103-6. doi: 10.1007/s00431-010-1280-x. Epub 2010 Sep 2.
[PMID: 20811907] [PMCID: 3016164] [DOI: 10.1007/s00431-010-1280-x]

Real name:

E-Mail:

Website:

Enter your comment. Wiki syntax is allowed:

Please fill all the letters into the box to prove you're human. D J P I᠎ S Please keep this field empty:

Subscribe to comments

Discussion