heterotaxy वाक्य
उदाहरण वाक्य
मोबाइल
- Mutations in this gene have been shown to cause heterotaxy.
- And mutations in another gene, lrd, can cause heterotaxy in mice.
- People with heterotaxy rarely live past young adulthood.
- In rarer cases such as situs ambiguus or heterotaxy, situs cannot be determined.
- There does not appear to be a screening method for prevention of heterotaxy syndrome.
- Biologists now know of two genes that can cause heterotaxy, one in humans and one in mice.
- Recent studies have shown higher rates of heterotaxy syndrome among Hispanic infants of racial disparities in heterotaxy syndrome.
- Recent studies have shown higher rates of heterotaxy syndrome among Hispanic infants of racial disparities in heterotaxy syndrome.
- Mutations in the human gene, ZIC3, have been found in four families with members who have heterotaxy.
- Individuals of Asian descent show a higher prevalence of heterotaxy syndrome in general than members of the Western world.
- Associated conditions include heterotaxy syndrome, intestinal malrotation, situs inversus, biliary atresia, and several cardiac malformations.
- But one time in 10, 000, in a condition known as heterotaxy, the embryo never distinguishes left from right.
- Mutations in this gene are associated with visceral heterotaxy-6, which implicates this gene in determination of left-right asymmetric patterning.
- Complete reversal of all organs is known as situs inversus, while reversal of some organs but not others is called situs ambiguus or heterotaxy.
- Although heterotaxy will never be cured, he said, a number of treatments can be developed if the genetic causes of the disorder are better understood.
- Mutation of ZIC3 is also associated with various heart defects, such as heart looping, however these are thought to represent a mild form of heterotaxy.
- Heterotaxy syndrome with atrial isomerism occurs in 1 out of every 10, 000 live births and is associated with approximately 3 % of congenital heart disease cases.
- Individuals with situs inversus or situs solitus do not experience fatal dysfunction of their organ systems, as general anatomy and clinically considered to have a form of heterotaxy syndrome.
- This type of congenital heart defect is associated with patients with Down syndrome ( trisomy 21 ) or heterotaxy syndromes . 45 % of children with Down syndrome have congenital heart disease.
- However, genetic testing in family members that display atrial isomerism or other cardiac malformations may help to discern risk for additional family members, especially in X-linked causes of heterotaxy syndrome.
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