Familial occurrence of congenital diaphragmatic hernia

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Congenital diaphragmatic hernia with familial occurrence in a Taiwanese pedigree.

Congenital diaphragmatic hernia (CDH) is a developmental defect that accounts for 8% of all major congenital anomalies and is associated with a high mortality rate despite optimal postnatal treatment. Its etiology is uncertain. We report a case of familial CDH in a Taiwanese family. We believe autosomal recessive inheritance is the possible genetic etiology of CDH in this family.

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Congenital diaphragmatic hernia.

Congenital diaphragmatic hernia (CDH) can be one of the most clinically challenging neonatal conditions. It occurs in 1 in 2-5000 live births in the UK with no predominance between the sexes. Herniation of abdominal contents into the thorax occurs, however it is the concomitant pulmonary hypoplasia and pulmonary hypertension that can be fatal. CDH was first described as an incidental finding at...

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Congenital Diaphragmatic Hernia

Congenital Diaphragmatic Hernia (CDH) is defined by the presence of an orifice in the diaphragm, more often left and posterolateral that permits the herniation of abdominal contents into the thorax. The lungs are hypoplastic and have abnormal vessels that cause respiratory insufficiency and persistent pulmonary hypertension with high mortality. About one third of cases have cardiovascular malfo...

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Congenital Diaphragmatic Hernia

Departments of Pediatrics and Pediatric Surgery, National Taiwan University Hospital, National Taiwan University Medical College, Taipei; and Department of Pediatrics, Cardinal Tien Hospital, Taipei Hsien. Received: 12 July 2000. Revised: 21 August 2000. Accepted: 21 December 2000. Reprint requests and correspondence to: Dr. Kuo-Inn Tsou Yau, Department of Pediatrics, Cardinal Tien Hospital, 36...

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Bilateral Congenital Diaphragmatic Hernia

Bilateral congenital diaphragmatic hernia (CDH) is a rare birth defect, with a poor prognosis. We describe a case of bilateral CDH discovered while repairing the right sided CDH. Diaphragmatic defect was repaired and a silo was applied on the abdominal wound to avoid abdominal compartment syndrome. The patient however died postoperatively due to severe pulmonary hypertension.

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ژورنال

عنوان ژورنال: Pediatric Surgery International

سال: 1996

ISSN: 0179-0358,1437-9813

DOI: 10.1007/bf00183756