RT Journal Article SR Electronic T1 Neonatal pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia JF Archives of Disease in Childhood - Fetal and Neonatal Edition JO Arch Dis Child Fetal Neonatal Ed FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health SP F226 OP F227 DO 10.1136/fn.87.3.F226 VO 87 IS 3 A1 Koppen, S A1 Korver, C R W A1 Dalinghaus, M A1 Westermann, C J J YR 2002 UL http://fn.bmj.com/content/87/3/F226.abstract AB A 3 week old infant presented with persistent hypoxaemia and was diagnosed with pulmonary arteriovenous malformations. Her family history was positive for hereditary haemorrhagic telangiectasia. She was treated successfully with coil embolotherapy at the age of 4 months. Transcatheter embolisation may be considered the primary treatment for pulmonary arteriovenous malformations in infancy.