Structured Summary
Abstract
Rare congenital deformity syndrome characterized by a combination of five anomalies as a result of neural tube defect. The five anomalies are a midline supraumbilical abdominal wall defect (e.g., OMPHALOCELE), a lower STERNUM defect, a congenital intracardiac defect, an anterior DIAPHRAGM defect, and a diaphragmatic PERICARDIUM defect (e.g., PERICARDIAL EFFUSION). Variants with incomplete and variable combinations of the defects are known. ECTOPIA CORDIS; CLEFT LIP; and CLEFT PALATE are often associated with the syndrome.
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Synonyms
8 entry terms
- Cantrell Haller Ravitch syndrome
- Cantrell Pentalogy
- Cantrell's Pentalogy
- Thoracoabdominal Syndrome
- Cantrells Pentalogy
- Pentalogy, Cantrell
- Pentalogy, Cantrell's
- Thoracoabdominal Syndromes
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2011
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Previous Indexing
- Abnormalities, Multiple (1984-2010)
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References
- National Library of Medicine. Pentalogy of Cantrell. Medical Subject Headings (MeSH). 2026. Unique ID D058502. http://id.nlm.nih.gov/mesh/2026/D058502
- Pentalogy of Cantrell. In: Wikipedia. https://en.wikipedia.org/wiki/Pentalogy_of_Cantrell
- Pentalogy of Cantrell. In: Wikidata. https://www.wikidata.org/wiki/Q7165022