RT Journal Article SR Electronic T1 Brain haemorrhage in five infants with coagulopathy JF Archives of Disease in Childhood JO Arch Dis Child FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health SP 1119 OP 1121 DO 10.1136/adc.88.12.1119 VO 88 IS 12 A1 E B A Vorstman A1 P Anslow A1 D M Keeling A1 G Haythornthwaite A1 H Bilolikar A1 M T McShane YR 2003 UL http://adc.bmj.com/content/88/12/1119.abstract AB Most intracranial haemorrhages in infants after the neonatal period are secondary to non-accidental injury. Occasionally brain haemorrhages in non-mobile infants are due to an inherited coagulopathy. This may often be diagnosed with a coagulation screen on admission. Little is known about the neurological outcome of infants in the latter group. Five infants are described who presented with acute spontaneous brain haemorrhage secondary to an inherited coagulopathy (n = 3) and vitamin K deficiency in α1 antitrypsin deficiency (n = 1) and Alagille’s syndrome (n = 1). Despite the critical clinical presentation and the severe imaging findings, these five infants made a good neurological recovery. Infants presenting with spontaneous ICH due to a significant (inherited) coagulopathy are usually easy to differentiate from non-accidental shaking injury; their bleeding pattern within the brain seems different from non-accidental shaking injury and neurodevelopment outcome appears better.