We report a female premature infant with bronchopulmonary dysplasia and Sandhoff disease. The clue for diagnosis was the fundoscopy examination. We discuss this rare disease with unusual presentation of intrauterine growth retardation, premature delivery, and bronchopulmonary dysplasia.

A malformed female infant is described. In addition to cardiac, renal, and skeletal (rib) anomalies, severe intrauterine growth retardation and distinct facial dysmorphism were present. The question is raised whether this child represents a new syndrome.

Background: There is an association between intrauterine growth retardation (IUGR) and subsequent development of diabetes mellitus, coronary artery disease hypertension during adult life. With this context, it vital to give attention about the patterns body proportion IUGR babies. The aim study was determine asymmetric distribution in contrast symmetric among babies with low birth weight (LBW)....