heterotaxy


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  • noun

Synonyms for heterotaxy

any abnormal position of the organs of the body

References in periodicals archive ?
At 17 weeks the mum and dad were told the sack had disappeared, but their baby had a condition known as complete heart block and further down the line, at 28 weeks, they were given the devastating news she had Heterotaxy Syndrome, which had caused a mirrored heart.
Heterotaxy was observed in only 5 of the 19 cases with cardiac defects, being much lower than the other previous prenatal series in which it was reported as 41-54% (3,8).
[9] Of all congenital heart defects, heterotaxy has the highest risk of familial recurrence.
Anderson, "Analysis of visceral heterotaxy according to splenic status, appendage morphology, or both," The American Journal of Cardiology, vol.
Many genes are responsible for the left-right development pathway in the human embryo, and any mutation of these genes causes left-right asymmetrical disorders such as heterotaxy and SIT.
In summary, AM is a rare, but important, cause of PH, and must be considered during the diagnostic work-up of PH in children, particularly when it is associated with heterotaxy syndrome.
He is functionally asplenic and will need to take prophylactic antibiotics the rest of his life to prevent and protect against sepsis, a huge risk of death for our kids in the heterotaxy community," she added.
TAPVR association with lesion like common AV canal, conotruncal anomalies, and systemic venous anomalies, mitral and pulmonary atresia characterize its association with heterotaxy patients1.
Situs ambiguous or heterotaxy implies a disordered organ arrangement in the chest or abdomen.
Takao, "Influence of genetic and maternal diabetes in the pathogenesis of visceroatrial heterotaxy in mice," Teratology, vol.
Heterotaxy syndrome is a general term that describes disruption in normal positioning of the visceral organs in the chest and abdomen.
A very serious syndrome that appears with this condition is called heterotaxy wherein many organs will not be in their usual places and may not work properly, it added.
This provides evidence that some cases of familial transposition are caused by mutations in laterality genes and therefore are part of the same disease spectrum of heterotaxy syndrome, and argues for an oligogenic or complex mode of inheritance in these pedigrees.