Introduction The renal arteries arise from abdominal aorta below the origin of superior mesenteric artery, on each side. Near the hilum of the kidney, each renal artery divides into anterior and posterior branch, which in turn divides into number of segmental arteries supplying the different renal segments. The presence of unusual branching patterns of the renal arteries is not uncommon. In 70%...

cleft lip and cleft palate are one of the most frequent congenital anomalies worldwide. this study was conducted in order to measure the frequency of cleft lip and palate among live births in akbar abadi hospital. this is a descriptive study, dealing with 57526 cases of live birth out of 59477 medical files in akbar abadi hospital from 2004 to 2008. all the collected data were recorded in speci...

maternal diabetes has teratogenic effects on the evolution of the fetal cardiovascular system; as a consequence, cardiovascular malformations are the most common anomalies in infants of diabetic mothers. the present study focuses on the association of all types of diabetes in mothers with the incidence of congenital cardiovascular malformations in their infants. in this retrospective case-contr...

BACKGROUND To evaluate the accuracy of helical computerized tomography urography (CTU) in diagnosing urinary tract disease. METHODS We collected 102 patients who underwent CTU from March 2001 to September 2002. The clinical symptoms of these patients included: flank pain or hematuria, which were clinically suggestive of urinary system disorders. All patients received CT scan with or without i...

PURPOSE To assess the regional patterns of infant mortality due to lethal congenital anomalies, and the potential reasons for the regional patterns. METHOD The study analyzed 2,507 infant deaths due to lethal congenital anomalies among 1,178,452 live births in 9 of the 12 Canadian provinces and territories from 1990 to 1995 recorded in Statistics Canada's live birth and death data bases. RE...

Congenital anomalies of the kidney and urinary tract (CAKUT) form a group of heterogeneous disorders that affect the kidneys, ureters and bladder, with frequent asynchronous presentations and multiple CAKUT associations in the same individual. Urinary tract formation is a complex process, dependent of the interaction of multiple genes and their sub-product. The same genic alterations can lead t...

BACKGROUND HDR syndrome (hypoparathyroidism, sensorineural deafness and renal disease) is an autosomal dominant condition, defined by the triad hypoparathyroidism, renal dysplasia and hearing loss. Hirschsprung (HSCR) disease is a variable congenital absence of ganglion cells of the enteric nervous system resulting in degrees of functional bowel obstruction. Rarer chromosomal anomalies are repo...

Edward’s syndrome is commonly known as the trisomy 18 syndrome. It a devastating genetic disorder that can be characterized by multiple congenital anomalies. About 50% babies with this do not survive beyond one week of age and approximately 95% does past first year life. The feature Syndrome involves in craniofacial, skeletal, cardiovascular, central nervous system genitourinary malformations. ...

background cutis marmorata telangiectatica congenita (cmtc) is a sporadic congenital skin vascular abnormality. significant number of patients has other congenital anomalies. case report we report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, right side of front of the trunk, whole back, glutei and both legs. besides, microretrognatia and asymm...