TY - JOUR 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 SP - F226 LP - F227 DO - 10.1136/fn.87.3.F226 VL - 87 IS - 3 AU - S Koppen AU - C R W Korver AU - M Dalinghaus AU - C J J Westermann Y1 - 2002/11/01 UR - http://fn.bmj.com/content/87/3/F226.abstract N2 - 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. ER -