Results 41 to 50 of about 18,119 (214)
Congenital aplasia of the optic chiasm and esophageal atresia: a case report
Introduction The complete absence of the chiasm (chiasmal aplasia) is a rare clinical condition. Hypoplasia of the optic nerve and congenital nystagmus are almost invariably associated characteristics.
Madonia Maurizio +5 more
doaj +1 more source
Background Esophageal atresia with or without a trachea–esophageal fistula occurs due to the failure of separation or incomplete development of the foregut.
Terutaka Tanimoto +3 more
doaj +1 more source
Anatomic Thoracoscopic Repair of Esophageal Atresia [PDF]
Background: The thoracoscopic approach to repair esophageal atresia (EA) with tracheoesophageal fistula (TEF) provides excellent view, allowing the most skillful surgeons to spare the azygos vein by performing the esophageal anastomosis over (on the ...
Al Tokhais +13 more
core +1 more source
Transthoracic single port with peroral assistance : an animal experiment to assess a less invasive technique for human esophageal atresia repair [PDF]
Prova tipográfica.Thoracoscopic repair of esophageal atresia has becoming the gold standard in many centers since it allows a better cosmetic result and avoids the musculoskeletal sequelae of a thoracotomy.
Coelho, Tiago Henriques +4 more
core +1 more source
Type-C esophageal atresia with double distal fistula (IIIb13)
Esophageal atresia (EA) is the most frequent congenital anomaly of the esophagus. According to Gross Classification, type-C esophageal atresia is the most common type.
César Ramírez-Martínez +8 more
doaj +1 more source
Anastomotic stricture is a common complication following repair of esophageal atresia with or without tracheo-esophageal fistula, affecting the long-term prognosis of survival.
Debarpito Mukherjee +3 more
doaj +1 more source
Due to the rarity of the association of esophageal and duodenal atresia, no consensus exists regarding the optimal treatment strategy. However, a staged approach is advised in order to reduce morbidities and improve survival.
Pieralba Catalano +7 more
doaj +1 more source
Dilated azygos arch mimicking an aortic arch anomaly during thoracic surgery [PDF]
Cardiovascular malformations are frequently associated in patients with esophageal atresia (EA). We observed azygos continuation mimicking an aortic arch anomaly in four newborns with type III EA.
Corsello, G. +4 more
core +1 more source
Esophageal atresia/tracheoesophageal fistula (EA/TEF) is the most common congenital anomaly of the upper gastrointestinal tract affecting 1 in 3,000 which could stem from a developmental anomaly of the foregut. The cause is not fully understood.
Suleen Raad +3 more
doaj +1 more source
Isolated congenital tracheal stenosis in a preterm newborn [PDF]
Severe tracheal stenosis, resulting in functional atresia of the trachea is a rare congenital malformation with an estimated occurrence of two in 100,000 newborns.
Ralph M. W. Rödel +2 more
core +2 more sources

