 Heterotaxy Syndrome
"Heterotaxy Syndrome" 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.
Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart isomerism; DEXTROCARDIA) and/or abnormal SPLEEN (e.g., asplenia and polysplenia). Irregularities with the central nervous system, the skeleton and urinary tract are often associated with the syndrome.
| Descriptor ID |
D059446
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| MeSH Number(s) |
C14.240.400.592 C14.280.400.592 C15.604.744.146 C16.131.077.401 C16.131.240.400.592
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| Concept/Terms |
Heterotaxy Syndrome- Heterotaxy Syndrome
- Heterotaxy Syndromes
- Syndrome, Heterotaxy
- Syndromes, Heterotaxy
Visceral Heterotaxy- Visceral Heterotaxy
- Heterotaxies, Visceral
- Heterotaxy, Visceral
- Visceral Heterotaxies
- Situs Ambiguus Viscerum
- Ambiguus Viscerum, Situs
- Ambiguus Viscerums, Situs
- Situs Ambiguus Viscerums
- Viscerum, Situs Ambiguus
- Viscerums, Situs Ambiguus
- Situs Ambiguus
- Ambiguus, Situs
Polysplenia Syndrome- Polysplenia Syndrome
- Polysplenia Syndromes
- Syndrome, Polysplenia
- Syndromes, Polysplenia
- Situs Ambiguus with Polysplenia
- Left Atrial Isomerism with Polysplenia
Right Atrial Isomerism- Right Atrial Isomerism
- Atrial Isomerism, Right
- Atrial Isomerisms, Right
- Isomerism, Right Atrial
- Isomerisms, Right Atrial
- Right Atrial Isomerisms
Asplenia Syndrome- Asplenia Syndrome
- Asplenia Syndromes
- Syndrome, Asplenia
- Syndromes, Asplenia
- Situs Ambiguus with Asplenia
- Right Atrial Isomerism with Asplenia
- Asplenia with Cardiovascular Anomalies
- Ivemark Syndrome
- Syndrome, Ivemark
Left Atrial Isomerism- Left Atrial Isomerism
- Atrial Isomerism, Left
- Atrial Isomerisms, Left
- Isomerism, Left Atrial
- Isomerisms, Left Atrial
- Left Atrial Isomerisms
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Below are MeSH descriptors whose meaning is more general than "Heterotaxy Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Heterotaxy Syndrome".
This graph shows the total number of publications written about "Heterotaxy Syndrome" by people in this website by year, and whether "Heterotaxy Syndrome" 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 |
|---|
| 2010 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2018 | 2 | 0 | 2 | | 2021 | 2 | 0 | 2 | | 2023 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Heterotaxy Syndrome" by people in Profiles.
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Barber AT, Shapiro AJ, Davis SD, Ferkol TW, Atkinson JJ, Sagel SD, Dell SD, Olivier KN, Milla CE, Rosenfeld M, Li L, Lin FC, Sullivan KM, Capps NA, Zariwala MA, Knowles MR, Leigh MW. Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype. Ann Am Thorac Soc. 2023 03; 20(3):397-405.
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Khan A, Pahl E, Koehl DA, Cantor RS, Kirklin JK, Rusconi P, Barnes AP, Azeka E, Everitt MD. Improved heart transplant survival for children with congenital heart disease and heterotaxy syndrome in the current era: An analysis from the pediatric heart transplant society. J Heart Lung Transplant. 2021 10; 40(10):1153-1163.
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Romanowicz J, Sinha P, Donofrio MT, Schidlow DN. Predicting Cardiac Anatomy, Physiology, and Surgical Management Based on Fetal Echocardiography in Heterotaxy Syndrome. Am J Perinatol. 2023 07; 40(10):1081-1087.
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Bove KE, Thrasher AD, Anders R, Chung CT, Cummings OW, Finegold MJ, Finn L, Ranganathan S, Kim GE, Lovell M, Magid MS, Melin-Aldana H, Russo P, Shehata B, Wang L, White F, Chen Z, Spino C, Magee JC. Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome. Am J Surg Pathol. 2018 12; 42(12):1625-1635.
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Kitano M, Hoashi T, Kakuta T, Fujimoto K, Miyake A, Kurosaki KI, Ichikawa H, Shiraishi I. Primary Draining Vein Stenting for Obstructive Total Anomalous Pulmonary Venous Connection in Neonates with Right Atrial Isomerism and Functional Single Ventricle Improves Outcome. Pediatr Cardiol. 2018 Oct; 39(7):1355-1365.
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Meyers ML, Crombleholme T. Prenatal MRI Diagnosis of Hirschsprung's Disease at 29 Weeks' Gestational Age in a Fetus with Heterotaxy and Polysplenia Syndrome. Fetal Diagn Ther. 2016; 40(3):235-240.
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Law YM, Mack CL, Sokol RJ, Rice M, Parsley L, Ivy D. Cardiopulmonary manifestations of portovenous shunts from congenital absence of the portal vein: pulmonary hypertension and pulmonary vascular dilatation. Pediatr Transplant. 2011 Dec; 15(8):E162-8.
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