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| content:alpha-1_antitrypsin_serum [2022/04/30 11:31] – administrator@icnapedia.org | content:alpha-1_antitrypsin_serum [2022/04/30 11:54] (current) – changed pubmed syntax administrator@icnapedia.org | ||
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| Late neonatal intracranial haemorrhage | Late neonatal intracranial haemorrhage | ||
| ==== Notes ==== | ==== 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)/ | + | * 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)/ |
| * AAT deficiency is a rare genetic disorder that can lead to a serious bleeding disorder in the neonatal period if not recognised on time | * AAT deficiency is a rare genetic disorder that can lead to a serious bleeding disorder in the neonatal period if not recognised on time | ||