Nghĩa của từ trisomy bằng Tiếng Việt

Hiện tượng thể ba

Đặt câu có từ "trisomy"

Dưới đây là những mẫu câu có chứa từ "trisomy", trong bộ từ điển Từ điển Y Khoa Anh - Việt. Chúng ta có thể tham khảo những mẫu câu này để đặt câu trong tình huống cần đặt câu với từ trisomy, hoặc tham khảo ngữ cảnh sử dụng từ trisomy trong bộ từ điển Từ điển Y Khoa Anh - Việt

1. Trisomy 21 affects chromosome 21.

Hiện tượng nhiễm sắc thể tam đồng 21 ảnh hưởng đến nhiễm sắc thể 21.

2. Trisomy 21 is a congenital defect causing mental retardation.

Chứng nhiễm sắc thể tam đồng 21 là khiếm khuyết bẩm sinh dẫn đến tình trạng chậm phát triển trí tuệ.

3. Trisomy-8 is a numerical chromosomal aberration. It's pathogenetic causality is uncertain.

4. Thus, Trisomy 21 is commonly known as Down syndrome.

Do đó, Trisomy 21 thường được gọi là hội chứng Down.

5. Broad Clavicles in trisomy 8 mosaicism: a new sign

6. Chromosome 14, Trisomy Mosaic is a rare chromosomal disorder in which Chromosome 14 appears three times (trisomy) rather than twice in some cells of the body

7. Further investigations for foetal and obstetric abnormalities other than trisomy 21, can be performed.

8. 23 Our findings also point to the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy

9. 24 One of their main findings is the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy

10. Q92.9 is a valid billable ICD-10 diagnosis code for Trisomy and partial trisomy of Autosomes, unspecified.It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021.

11. The accelerated aging suggest that trisomy 21 increases the biological age of tissues, but molecular evidence for this hypothesis is sparse.

12. Trisomy 13 is associated with multiple Abnormalcies, including terrible mental defects and defects of the encephalon that lead to ictuss, hearing loss, and optic Abnormalcies

13. AMNIOCENTESIS, ANOMALIES CONGÉNITALES, CONGENITAL ANOMALIES, DIMERIC INHIBIN-A, GROSSESSE/ACCOUCHEMENT, HEALTH SERVICES, LES SERVICES DE SANTÉ, PAPP-A, PREGNANCY/BIRTH, PRENATAL SCREENING, REPRODUCTION/GROSSESSE, REPRODUCTION/PREGNANCY, SERUM BIOCHEMISTRY MARKERS, TRISOMY 21 Abstract:

14. The partial trisomy 10q of the proband had induced mental retardation, severe retardation of growth, ocular anomalies, agenesis of the palate, low implantation of the ears, micrognathia bone anomalies and cardiac malformation.

15. The best performing screening tests are able to identify more than 90 % of trisomy 21 cases with a 5 % rate of false positives but positive screening results require confirmation with diagnostic testing, such as amniocentesis or chorionic villus sampling (CVS).

16. Most of these abnormalities had previously been described in prenatally diagnosed cases of partial or complete trisomy 17p [6, 7], except the cystic dilation of the Aqueductus Sylvii associated with dilation of the 4th ventricle, and this is a new observation.