triploidy

doctors diagnosed the fetus with triploidy during the routine ultrasound scan.

triploidy is a rare chromosomal abnormality characterized by three sets of chromosomes.

the patient decided to terminate the pregnancy after receiving the triploidy diagnosis.

most cases of triploidy result in spontaneous miscarriage during the first trimester.

genetic counseling is recommended for parents to understand the causes of triploidy.

distinguishing between partial molar pregnancy and triploidy requires careful histopathological examination.

pathologists identified triploidy as the cause of the intrauterine fetal demise.

the prognosis for live birth is extremely poor for fetuses with complete triploidy.

advanced maternal age is not considered a significant risk factor for triploidy.

distinctive physical malformations often suggest the presence of triploidy in the fetus.

karyotyping confirmed the presence of 69 chromosomes indicating triploidy syndrome.

prenatal screening tests can sometimes indicate potential risks for triploidy.