نتایج جستجو برای: associated anomalies
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background: aphallia or penile agenesis is a rare malformation accompanying with no phallus. this anomaly is extremely rare with abnormality of urogenital system and psychological consequences. its outbreak is estimated 1 out of 10-30 million births.case: reviewing 3 cases of male external genitalia agenesis, which associated with multiple anomalies of musculoskeletal, cardiovascular and genito...
Introduction: Orofacial clefts are among the most common congenital anomalies. Patients presenting with orofacial clefts often require surgery or other complex procedures. A cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. The reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...
Background: Imperforate anus is a common anomaly associated with many other anomalies. The aim of this study is determining the frequency of associated anomalies in children with imperforated anus. Methods: This retrospective, cross sectional study was conducted by 245 neonates and children (137 male, 105 female and 3 ambiguous genitalia) with imperforated anus diagnosis, in Ali-Asghar hosp...
From October 1977 to December 1988, 108 neonates born with esophageal atresia (EA) and/or a tracheoesophageal fistula (TEF) were treated at the Bristol Royal Hospital for Sick Children. An incidence of I :4000-4500 live births was noted. 1I2.4% had the common- type anomaly, 5.5% had pure esophageal atresia, and 6.5% had an H-type anomaly. 2.8% had upper and lower fistulae and 2.8% had uppe...
introduction: orofacial clefts are among the most common congenital anomalies. patients presenting with orofacial clefts often require surgery or other complex procedures. a cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. the reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...
Introduction: Albinism refers to a group of inherited conditions. People with albinism have little or no pigment in their eyes, skin and hair. Albinism doesn't occur together with other anomalies with the exception of a case associated with microcephaly and digital hypoplasia. VACTERL is a syndrome consisting of multiple anomalies such as vertebral anomalies, anal atresia, cardiac anomaly, ...
from october 1977 to december 1988, 108 neonates born with esophageal atresia (ea) and/or a tracheoesophageal fistula (tef) were treated at the bristol royal hospital for sick children. an incidence of i :4000-4500 live births was noted. 1i2.4% had the common- type anomaly, 5.5% had pure esophageal atresia, and 6.5% had an h-type anomaly. 2.8% had upper and lower fistulae and 2.8% had upper fis...
Introduction: Beckers’s nevus is a cutaneous hamartoma which usually appears as a circumscribed hyperpigmentation with hypertrichosis. It usually presents unilaterally and the usual site is shoulder and scapula. It is rarely congenital and it is usually noticed first during adolescence. Case Report: Herein, we report a congenital bilateral large Becker’s nevus with positive familial history ...
Developmental defect of Mullerian duct is a congenital malformation characterized by anomalies in famale upper genital organs. As the anomaly is associated with obstruction of the duct, other congenital anomalies of urinary tract specially ipsilateral ranal agenesis are common. This anomaly is often discovered in adolescent period and is usually asymptomatic until puberty. To discover this anom...
introduction congenital microgastria is an extremely rare anomaly, which is due to failure of gastric development, and causes a tubular stomach with reduced capacity. it is almost always associated with other congenital anomalies. case presentation the patient was a two-month-old boy with microgastria in association with gastroesophageal reflux, tracheomalacia, and limb defect. discussion most ...
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