Hernias, Diaphragmatic, Congenital
"Hernias, Diaphragmatic, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Protrusion of abdominal structures into the THORAX as a result of embryologic defects in the DIAPHRAGM often present in the neonatal period. It can be isolated, syndromic, nonsyndromic or be a part of chromosome abnormality. Associated pulmonary hypoplasia and PULMONARY HYPERTENSION can further complicate stabilization and surgical intervention.
Descriptor ID |
D065630
|
MeSH Number(s) |
C16.131.433 C23.300.707.500.116
|
Concept/Terms |
Hernias, Diaphragmatic, Congenital- Hernias, Diaphragmatic, Congenital
- Unilateral Agenesis of Diaphragm
- Diaphragm Unilateral Ageneses
- Diaphragm Unilateral Agenesis
- Congenital Diaphragmatic Hernias
- Congenital Diaphragmatic Hernia
- Diaphragmatic Hernia, Congenital
- Diaphragmatic Hernias, Congenital
- Hernia, Congenital Diaphragmatic
- Hernias, Congenital Diaphragmatic
- Agenesis of Hemidiaphragm
- Hemidiaphragm Ageneses
- Hemidiaphragm Agenesis
- Congenital Diaphragmatic Defect
- Congenital Diaphragmatic Defects
- Defect, Congenital Diaphragmatic
- Defects, Congenital Diaphragmatic
- Diaphragmatic Defect, Congenital
- Diaphragmatic Defects, Congenital
Morgagni Hernias- Morgagni Hernias
- Hernias, Morgagni
- Morgagni's Hernias
- Hernias, Morgagni's
- Morgagnis Hernias
|
Below are MeSH descriptors whose meaning is more general than "Hernias, Diaphragmatic, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Hernias, Diaphragmatic, Congenital".
This graph shows the total number of publications written about "Hernias, Diaphragmatic, Congenital" by people in this website by year, and whether "Hernias, Diaphragmatic, Congenital" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 1 | 0 | 1 |
1995 | 1 | 0 | 1 |
1996 | 1 | 0 | 1 |
1997 | 1 | 0 | 1 |
2000 | 0 | 1 | 1 |
2001 | 1 | 0 | 1 |
2002 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2004 | 0 | 1 | 1 |
2005 | 1 | 1 | 2 |
2006 | 1 | 2 | 3 |
2007 | 2 | 1 | 3 |
2008 | 2 | 2 | 4 |
2009 | 3 | 0 | 3 |
2010 | 1 | 2 | 3 |
2011 | 5 | 2 | 7 |
2012 | 5 | 3 | 8 |
2013 | 3 | 0 | 3 |
2014 | 8 | 0 | 8 |
2015 | 16 | 0 | 16 |
2016 | 7 | 0 | 7 |
2017 | 6 | 1 | 7 |
2018 | 13 | 1 | 14 |
2019 | 6 | 0 | 6 |
2020 | 7 | 0 | 7 |
2021 | 15 | 1 | 16 |
2022 | 9 | 0 | 9 |
2023 | 12 | 0 | 12 |
2024 | 2 | 0 | 2 |
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Below are the most recent publications written about "Hernias, Diaphragmatic, Congenital" by people in Profiles.
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First-year growth trajectory and early nutritional requirements for optimal growth in infants with congenital diaphragmatic hernia: a retrospective cohort study. Arch Dis Child Fetal Neonatal Ed. 2024 Feb 19; 109(2):166-172.
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Surfactant Therapy in Congenital Diaphragmatic Hernia and Fetoscopic Endoluminal Tracheal Occlusion. J Surg Res. 2024 Apr; 296:239-248.
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Pathogenesis and Physiologic Mechanisms of Neonatal Pulmonary Hypertension: Preclinical Studies. Clin Perinatol. 2024 Mar; 51(1):21-43.
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Oxygen saturation index: an adjunct for oxygenation index in congenital diaphragmatic hernia. J Perinatol. 2024 Mar; 44(3):354-359.
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Using MRI-derived observed-to-expected total fetal lung volume to predict lethality in fetal skeletal dysplasia. Pediatr Radiol. 2024 01; 54(1):43-48.
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Organization of care of infants with congenital diaphragmatic hernia-Building a high-functioning CDH program. J Perinatol. 2024 Mar; 44(3):339-347.
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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects. Am J Hum Genet. 2023 10 05; 110(10):1787-1803.
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Molecular insights using spatial transcriptomics of the distal lung in congenital diaphragmatic hernia. Am J Physiol Lung Cell Mol Physiol. 2023 10 01; 325(4):L477-L486.
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Core outcome set for perinatal interventions for congenital diaphragmatic hernia. Ultrasound Obstet Gynecol. 2023 09; 62(3):374-382.
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Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. Eur J Hum Genet. 2023 10; 31(10):1117-1124.