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Omphalocele (exomphalos) represents one of the most frequent congenital abdominal wall defects. It presents as a defect of inconstant size and is located on the midline, at the base of the umbilical cord, the skin, fascia, and abdominal muscles being absent at this level. Omphaloceles are classified as liver-containing or non-liver-containing, the latter containing primarily bowel loops.

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Background: When esophagocardiomyotomy (ECM) is performed for achalasia, a complementary antireflux procedure of the surgeon's choice is usually performed to minimize postoperative gastroesophageal reflux. This retrospective analysis describes patients after laparoscopic ECM, most of whom had a modified Dor fundoplication.

Methods: Between 1994 and 2001, 81 patients with achalasia of the esophagus had laparoscopic ECM.

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Pallister-Killian syndrome: difficulties of prenatal diagnosis.

Prenat Diagn

June 2002

Laboratoire de Cytogénétique, Hôpital de Hautepierre, Strasbourg, France.

The first prenatal diagnosis of Pallister-Killian syndrome (PKS) was reported by Gilgenkrantz et al. in1985. Since this report, about 60 prenatal cases have been reported but both sonographic and cytogenetic diagnoses remain difficult.

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Spigelian herniae: presentation, diagnosis and treatment.

J R Coll Surg Edinb

August 1996

Department of Surgery, Whiston Hospital, Prescot, Merseyside, UK.

A personal series of 19 patients (8 males), mean age 62.4 years (range 21-83 years) with a spigelian hernia [right-sided in eight patients (42.1%)] is presented.

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Congenital and acquired lung hernias.

J Thorac Imaging

September 1996

Department of Radiology, Loyola University Medical Center, Maywood, Illinois 60153, USA.

Lung hernia is defined as a protrusion of lung parenchyma beyond the confines of the musculoskeletal thorax. Lung hernias can be classified according to location (i.e.

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