Congenital lobar emphysema (CLE) is a rare developmental malformation that presents as neonatal respiratory distress and can be successfully managed with prompt intervention. Hyperinflation of the affected lobe mediastinal shift characteristic radiological finding. However, etiology mostly remains unknown. Here, we report case CLE microscopically revealed bronchial cartilaginous hypoplasia an u...

Acalvaria defined as absent skull bones, is an extremely rare congenital anomaly with only a handful of cases reported in literature. In this report we presented a male newborn case of acalvaria referred to our hospital (Shahid Motahari hospital of Urmia, Iran). The condition per se has been described as having high mortality rate. Very few living cases, less than ten, have been reported till now.

OBJECTIVE To identify the referral factors for fetal echocardiography which are associated with congenital cardiac defects in the fetus. STUDY DESIGN Cross-sectional descriptive study. PLACE AND DURATION OF STUDY Radiology Department, CMH, Rawalpindi, from January 2007 to November 2010. METHODOLOGY All patients referred for fetal echocardiography with one or more risk factors for the deve...

background congenital pulmonary lesions may be diagnosed through ultrasonographic screenings or be revealed as causes of respiratory distress in the neonatal period and infancy. less commonly, they are detected as incidental features. objectives our study represents the diversity of congenital pulmonary lesions and their characteristics during an 11-year period in a referral teaching children’s...

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...

Sixteen patients aged between one day to 18 years with Ebstein's malformation of the tricuspid valve were studied with ultrasound. The findings were compared with a group of 74 patients without Ebstein's malformation. Two features were considered specific for Ebstein's malformation: 1) ability to record the anterior tricuspid leaflet (ATL) farther to the left of the left sternal border than in ...

A complex congenital cardiac malformation in a female patient was evaluated several times by angiocardiography and echocardiography in childhood but a definite diagnosis was not established. Segmental analysis of the heart and the great vessels by magnetic resonance imaging when the patient was 34, however, showed a double outlet left ventricle in which the aorta was situated anterior to and to...

Double orifice mitral valve (DOMV) is an uncommon congenital heart defect. The isolated occurrence of this anomaly is very rare and, more often, is associated with another congenital malformation, dominated by atrioventricular canal defects (AVCD). Mitral insufficiency and/or stenosis may complicate this malformation. Treatment may be summarized as abstention, surgical valve repair, or valve re...

BACKGROUND Although screening for congenital heart malformations is part of the child health care programme in several countries, there are very few published evaluations of these activities. This report is concerned with the evaluation of this screening at the Dutch Child Health Centres (CHC). METHODS All consecutive patients, aged between 32 days and 4 years, presented at the Sophia Childre...

OBJECTIVE Left isomerism, also called polysplenia, is a laterality disturbance associated with with paired leftsidedness viscera and multiple small spleens. Left isomerism, heart congenital abnormalities and gastrointestinal malformation are strongly associated. METHODS We present a case of prenatal diagnosis of left isomerism in a fetus with a structurally normal heart. CONCLUSION Left iso...