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Congenital diaphragmatic hernia

Seminars in Pediatric Surgery, 2010
Congenital diaphragmatic hernia (CDH) is a congenital anomaly consisting of a posterolateral defect in the diaphragm also known as a Bochdalek hernia. It occurs in 1 in 2000 to 3000 newborns and is associated with a variable degree of pulmonary hypoplasia (PH) and persistent pulmonary hypertension (PPH).
Keijzer, Richard, Puri, P
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Congenital Diaphragmatic Hernia

Surgical Clinics of North America, 1981
Surgical intervention for congenital diaphragmatic hernia is urgent, but success depends more on preoperative and postoperative management of the associated physiologic derangements. Survival seems to depend on the condition of the lungs at birth. In the future, correction of congenital diaphragmatic hernia in utero may be possible.
M R, Harrison, A A, de Lorimier
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Congenital diaphragmatic hernia

Pediatric Radiology, 2020
Congenital diaphragmatic hernia (CDH) is a potentially severe anomaly that should be referred to a fetal care center with expertise in multidisciplinary evaluation and management. The pediatric radiologist plays an important role in the evaluation of CDH, both in terms of anatomical description of the anomaly and in providing detailed prognostic ...
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Congenital Diaphragmatic Hernia

New England Journal of Medicine, 2017
A baby girl was delivered by cesarean section at 36 weeks of gestation because of an antenatal diagnosis of congenital diaphragmatic hernia.
Jared, Klein, Megan, Sirota
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Congenital diaphragmatic hernia

Early Human Development, 2014
There is a paucity of level 1 and level 2 evidence for best practice in surgical management of CDH. Antenatal imaging and prognostication is developing. Observed to expected lung-to-head ratio on ultrasound allows better predictive value over simple lung-to-head ratio.
Lisette, Leeuwen, Dominic A, Fitzgerald
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Congenital Diaphragmatic Hernia

Surgical Clinics of North America, 1985
Congenital diaphragmatic hernia continues to be a critical problem in neonatal surgery. Despite the apparent simplicity of the anatomic defect, the physiology is complex, and survival remains uncertain. Surgical success has been achieved, but we recognize that the barrier to survival is pulmonary parenchymal and vascular hypoplasia as well as the ...
M L, Cullen, M D, Klein, A I, Philippart
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Congenital diaphragmatic hernia

Clinical Genetics, 1980
Background—congenital diaphragmatic hernia (CDH) has a reported incidence of 1 in 2500 to 1 in 4000 live births with an estimated 30 % spontaneous abortion rate.
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CONGENITAL DIAPHRAGMATIC HERNIA

Archives of Surgery, 1954
DURING the past seven years we have observed 33 cases of congenital diaphragmatic hernias at the Children's Memorial Hospital, 31 of which have undergone surgical repair. During the course of this experience, several important points in the care of these patients have been forcefully impressed upon us.
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Congenital Diaphragmatic Hernia

Archives of Surgery, 1967
BETWEEN 1948 and 1966, the incidence of congenital diaphragmatic hernias at the John Gaston Hospital in Memphis, Tenn, has been 1/7,000 live births. The total number of cases at the teaching hospitals associated with the University of Tennessee averaged approximately two cases per year during this interval; thus, the condition is uncommon even in large
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Congenital Diaphragmatic Hernia

The Indian Journal of Pediatrics, 2000
Over the last two decades there has been a constant improvement in the understanding of the pathophysiology of Congenital Diaphragmatic Hernia (CDH) and its management. However, the ideal treatment remains elusive. The earlier management strategy of immediate surgery is replaced by the principle of physiological stabilisation and delayed surgery ...
M, Arora   +3 more
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