PT  - JOURNAL ARTICLE
AU  - S Koppen
AU  - C R W Korver
AU  - M Dalinghaus
AU  - C J J Westermann
TI  - Neonatal pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia
AID  - 10.1136/fn.87.3.F226
DP  - 2002 Nov 01
TA  - Archives of Disease in Childhood - Fetal and Neonatal Edition
PG  - F226--F227
VI  - 87
IP  - 3
4099  - http://fn.bmj.com/content/87/3/F226.short
4100  - http://fn.bmj.com/content/87/3/F226.full
SO  - Arch Dis Child Fetal Neonatal Ed2002 Nov 01; 87
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.