RT Journal Article SR Electronic T1 Hemifacial microsomia with pulmonary hypoplasia JF BMJ Case Reports FD BMJ Publishing Group Ltd SP bcr0420091759 DO 10.1136/bcr.04.2009.1759 VO 2010 A1 Inusha Panigrahi A1 Rashmi Ranjan Das A1 Ram Kumar Marwaha YR 2010 UL http://casereports.bmj.com/content/2010/bcr.04.2009.1759.abstract AB Hemifacial microsomia (HFM) is the second most common facial anomaly after cleft lip and palate. HFM is characterised by facial asymmetry, microtia, preauricular tags, macrostomia and cardiac defects. The majority of cases are sporadic, although autosomal dominant and recessive modes of inheritance have been reported. Here, the case of an 11-month-old boy with HFM and pulmonary hypoplasia, which is a rare association, is described. Pulmonary hypoplasia was detected during investigation of the patient for associated anomalies. He is currently on follow-up in the genetic clinic.