نتایج جستجو برای: congenital anomaly
تعداد نتایج: 151428 فیلتر نتایج به سال:
a fifteen-year-old torkaman girl with turner's mosaic kariotype is presented. she has had congenital esophageal stenosis with severe dysphagia since birth and iron deficincy anemia in addition to other classical features of the syndrome. according to author's knowledge this is the first report of a new congenital structural gastrointestinal anomaly with this disease.
Background: Ankyloblepharon filiforme adnatum is a rare congenital anomaly characterized by partial or complete adhesion of upper and lower eyelids. This condition is usually observed as an isolated finding; however, it is often associated with other anomalies or a well-defined syndrome. The etiology of this defect has not been identified yet. Case Presentation: Herein, we reported the case of...
OBJECTIVE To assess the public health consequences of the rise in multiple births with respect to congenital anomalies. DESIGN Descriptive epidemiological analysis of data from population-based congenital anomaly registries. SETTING Fourteen European countries. POPULATION A total of 5.4 million births 1984-2007, of which 3% were multiple births. METHODS Cases of congenital anomaly inclu...
Congenital anomalies that are diagnosed in at least 120,000 US infants every year are the leading cause of infant death and contribute to disability and pediatric hospitalizations. Several large-scale epidemiologic studies have provided substantial evidence of an association between congenital anomalies and cancer risk in children, suggesting potential underlying cancer-predisposing conditions ...
the majority of coronary artery fistulas (cafs) are congenital. the anomaly accounts for 0.4% of congenital heart defects and approximately 50% of pediatric coronary vasculature anomalies. twenty percent of people with congenital cafs have other concomitant cardiac anomalies, most frequently aortic and pulmonary atresia and patent ductus arteriosus. it is worthy of note that caf with the tetral...
Background: Handicapped subjects have special social and clinical needs that should be observed. The present study was designed to survey the incidence of congenital anomalies in a rural population aged 5- 19 years in Rafsanjan. Materials and methods: In a descriptive study, we included 1356 subjects who were randomly selected through rural population of Rafsanjan. The incidence of congenit...
Orthotopic multicystic dysplastic kidney with crossed fused ectopia is a rare congenital anomaly. This congenital anomaly may give an appearance of a solitary kidney morphology during the initial imaging evaluation. A solitary kidney should be carefully evaluated for the presence of duplication, horseshoe configuration, or crossed renal ectopy. Vesicoureteral reflux is a common finding associat...
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