====== Alpha-1 antitrypsin, serum ======
Late neonatal intracranial haemorrhage	 	
==== Notes ====
  * 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[(:cite:20811907>{{pmid>long:20811907}})]. 
  * AAT deficiency is a rare genetic disorder that can lead to a serious bleeding disorder in the neonatal period if not recognised on time

==== References ====
~~REFNOTES~~
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