The Poland syndrome is a rare anomaly. It consists of unilateral absence or hypoplasia of the pectoralis muscle, most frequently involving the sternocostal portion and a variable degree of ipsilateral hand and digit anomalies. The combination of Poland syndrome and dextrocardia is uncommon. We describe a case of Poland syndrome with dextrocardia and Patent ductus arteriosus.

UNLABELLED The myocardial perfusion scintigraphy acquisition and analysis present some technical differences in the rare dextrocardia cases. Here we report a case of a 38 year-old woman with dextrocardia who had been applied myocardial perfusion scintigraphy. Presented case showed that the thoracic and abdominal organs had a mirror image with situs inversus totalis type dextrocardia. The incide...

Turner syndrome is a sex-chromosome disorder occurring in one out of 2500 female births and characterized by growth retardation, gonadal dysgenesis and cardiovascular anomalies. The 45, XO karyotype is the most frequent type of this disease. Herein, we report on a 6-year-old girl with Turner syndrome and 45, XO karyotype presenting with short stature. She had dextrocardia and hiatal hernia. To ...

Poland Syndrome is a congenital disorder characterised by hypoplasia of the pectoral muscles along with upper extremity deformities. We encountered a patient with Poland syndrome associated with dextrocardia and also failed pectus excavatum repairs who presented to us with symptomatic ischaemic heart disease requiring intervention. He underwent successful off-pump coronary artery bypass surgery...

Situs inversus with dextrocardia is a rare congenital anomaly. Azoospermia and situs inversus may be encountered in ciliary dyskinesia syndromes. We report the case of a 30-year-old male who manifested situs inversus totalis, dextrocardia and azoospermia with maturation arrest at primary spermatogenesis who presented with liver abscess. The patient responded well to treatment with i.v. metronid...

Omphalocele is frequently associated with many other congenital malformations. In cardiac anomalies, association of omphalocele with dextrocardia has been rarely noticed before. We present here a child with dextrocardia and omphalocele alongwith a brief review of the literature on this rare association.

background: dextrocardia is a congenital anomaly, which may have coexistent coronary artery disease (cad), arrhythmias and conventional indications for device therapy. however, the implantation of transvenous leads can be technically challenging and the approach needs to be tailored to the patient's individual anatomy. case presentation: a 54-year-old male with dextrocardia situs inversus ...

IN CONGENITAL dextrocardia the problem is frequently whether dextroversion or a mirror-image dextrocardia is present. In the former the atria preserve their usual relationship in the frontal plane but the left ventricle lies anterior to the right. In mirror-image dextrocardia there is atrial inversion and the right ventricle lies anterior to the left. The electrocardiographic findings are gener...

T incidence of coronary artery disease (CAD) in those with situs inversus (SI) is similar to that in the general population.1 Dextrocardia with complete SI occurs in approximately one per 10,000 live births,2 and is accompanied by congenital heart disease (usually transposition of the great vessels) in only 3-5% of cases.3 Patient having this anomaly and presenting with myocardial infarction (M...