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Congenital diaphragmatic hernia

โœ Scribed by S. Nour; E. Wing; N. Pereira; Mr A. E. MacKinnon

Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
177 KB
Volume
76
Category
Article
ISSN
0007-1323

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๐Ÿ“œ SIMILAR VOLUMES

Outcome of congenital diaphragmatic hern
Outcome of congenital diaphragmatic hernia
โœ M.W. Beresford; N.J. Shaw ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 280 KB ๐Ÿ‘ 1 views

The outcome of congenital diaphragmatic hernia (CDH) differs for different stages of the fetus or infant's life (i.e., antenatal, immediate postnatal, and postoperative). Assessing combined data from nonrandomized studies is technically difficult. Following recognized methods of reviewing such trial

Congenital diaphragmatic hernia in WAGR
Congenital diaphragmatic hernia in WAGR syndrome
โœ D.A. Scott; M.L. Cooper; P. Stankiewicz; A. Patel; L. Potocki; S.W. Cheung ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 88 KB ๐Ÿ‘ 2 views

## Abstract Wilms tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome involving the Wilms tumor 1 gene (__WT1__), the paired box gene 6 (__PAX6__), and possibly other genes on chromosome 11p13. __WT1__ is required for normal format

Delayed surgery for congenital diaphragm
Delayed surgery for congenital diaphragmatic hernia
โœ D. W. Goh; Mr. D. P. Drake; R. J. Brereton; E. M. Kiely; L. Spitz ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 347 KB ๐Ÿ‘ 2 views

The mortality rate was 33 per cent. Preoperative stabilization was achieved in 47 patients, all of whom survived initial treatment, although two died later. Stabilization could not be achieved in 20 neonates, all of whom died within 3 days of birth, 18 without undergoing operation and two after earl

Congenital diaphragmatic hernia misdiagn
Congenital diaphragmatic hernia misdiagnosed as tension pneumothorax
โœ M. E. Coren; M. Rosenthal; A. Bush ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 113 KB ๐Ÿ‘ 1 views

Drainage of the pleural space is undertaken as an emergency when there is respiratory distress and the radiological appearance of mediastinal shift. We present two cases in which the initial diagnosis was tension pneumothorax and chest drains were inserted. In both cases, the diagnosis turned out to

STRUCTURAL CHROMOSOME ANOMALIES IN CONGE
STRUCTURAL CHROMOSOME ANOMALIES IN CONGENITAL DIAPHRAGMATIC HERNIA
โœ DAVID T. HOWE; MARK D. KILBY; HATEM SIRRY; GILLIAN M. BARKER; EILEEN ROBERTS; E. ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 479 KB ๐Ÿ‘ 2 views

In order to determine the outcome and associated chromosomal and structural anomalies in fetuses diagnosed in utero as having a congenital diaphragmatic hernia, we reviewed 48 consecutive cases referred to our regional Fetal Diagnostic Unit between 1988 and 1995. All babies were delivered in units w