ABSTRACT
Tectocerebellar dysraphia is a rare constellation of malformations comprising of occipital encephalocele, aplasia of the cerebellar vermis and deformity of the tectum. We describe a 7 month old infant who presented with tectocerebellar dysraphia associated with double outlet right ventricle, pulmonary stenosis and abdominal situs inversus. This association has not been reported in the literature, to the best of our knowledge.
Subject(s)
Abnormalities, Multiple , Adult , Cerebellum/abnormalities , Double Outlet Right Ventricle/complications , Encephalocele/pathology , Female , Heart Defects, Congenital/pathology , Heart Ventricles/abnormalities , Humans , Infant , Levocardia/complications , Magnetic Resonance Imaging , Male , Situs Inversus/pathologyABSTRACT
Levocardia with situs inversus is a rare condition. We present the case of a fourteen-year-old boy with congenital cyanotic heart disease, isolated levocardia and splenic abscess. It is the first report of both these conditions occurring in the same person.
Subject(s)
Abdominal Abscess/complications , Adolescent , Comorbidity , Cyanosis/complications , Heart Defects, Congenital , Humans , Levocardia/complications , Male , Situs Inversus/complications , Splenic Diseases/complicationsABSTRACT
We report a patient with isolated levocardia without cardiac or splenic defects associated with duodenal membrane.