Cor triatriatum is a rare congenital cardiac malformation and it usually refers to the left atrium. We report an unusual case of cor triatriatum in a 33 - year old woman presented with congestive heart failure caused by left ventricular systolic dysfunction.

Common atrium is a rare congenital heart disease characterized by complete absence of the interatrial septum, and is commonly accompanied by malformation of the atrioventricular valve. Most patients with common atrium experience symptoms during childhood. Here, we describe a patient with common atrium who experienced his first obvious symptom at 48 years of age.

Accessory mitral valve tissue is a rare congenital malformation. It can be found isolated or in combination with other cardiac anomalies and is usually detected in early childhood. We describe the case of a 74-year-old asymptomatic patient who was referred to our clinic for the evaluation of a heart murmur.

A case of trisomy 9 showing a complex cardiac malformation is presented with a review of other published cases. A distinct trisomy 9 syndrome can be recognised with intrauterine growth retardation, short survival, consistent facial dysmorphism, congenital heart disease, and abnormalities of the skeletal, genital, and renal systems. There is no evidence for a maternal age effect.

background: today there is a rise in the number of newborns conceived by artificial reproductive techniques (art). numerous studies have been performed on the perinatal outcome of these pregnancies. however, there is limited data about the condition of health of these newborns in iran. objective: regarding the higher prevalence of probable complications and symptomatic congenital anomalies, we ...

We present a case of disseminated intracranial infection by Candida albicans in a 5-year-old girl who had fever and a change of consciousness after surgery for complex congenital heart malformation. MR imaging revealed multiple small ring-enhancing hemorrhagic abscesses. One year after antifungal treatment, the abscesses and ventriculomegaly were almost completely resolved. The patient was disc...

Hemi-truncus arteriosus is a rare congenital cardiovascular malformation. It usually presents in infancy and leads to development of progressive pulmonary vascular disease, heart failure, and death. We report a case of hemi truncus arteriosus in a 12-day-old neonate who was successfully managed at our institute.

The Arnold-Chiari malformation is a congenital abnormality of CNS, characterized by downward displacement the parts of the cerebellum, fourth ventricle, pons and medulla oblongata into the spinal canal. This malformation is one of causative factor of death in neonates and infants. A thorough understanding of the direct and indirect sonographic findings is necessary for diagnosis of Chiari II ma...

The two cases reported illustrate an uncommon type of partial inversion of the viscera, in which the abdominal organs alone are transposed while the heart remains in its normal position. Both were suffering from congenital heart disease, and a subsequent search brought to light several further reports of cardiac malformation associated with a similar transposition of the viscera. This combinati...