Braddock syndrome Braddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect. ICD10:Q87.8 MESH:C564244 MONDO:0012032 OMIM:608406 Orphanet:52047 SCTID:720575002 UMLS:C1842082 UMLS:C4303988 VATER-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency genetic hypertension syndrome with pulmonary hypertension as a major feature genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability