Trisomy

Trisomy can occur spontaneously, or it can be inherited from a parent.

Trisomy 21 is a genetic condition where there is an extra copy of the chromosome 21.

Trisomy of chromosome 13 is known as Patau syndrome.

Trisomy 8, also known as Warkany syndrome 2, is a rare chromosomal disorder that can cause a wide range of symptoms.

Early detection and intervention can help improve outcomes for individuals with trisomy.

Babies with trisomy may have physical abnormalities, such as heart defects.

Trisomy can affect any chromosome, but it is most common with chromosomes 13, 18, and 21.

The risk of trisomy increases as the mother's age increases.

Some people with trisomy may experience developmental delays and intellectual disabilities.

There is currently no cure for trisomy, and treatment focuses on managing symptoms.

Trisomy 21 is commonly known as Down syndrome.

Trisomy is caused by a chromosomal abnormality and is not related to environmental factors.

Trisomy 16 is the most common chromosomal abnormality found in miscarriages.

There is no cure for trisomy, but treatment can help alleviate symptoms and improve quality of life.

Doctors can test for trisomy using amniocentesis or chorionic villus sampling.

Babies born with trisomy 18 often have severe intellectual disability and health problems.

In some cases, trisomy can be fatal in the womb or shortly after birth.

Trisomy occurs when there are three copies of a chromosome instead of the usual two.

Trisomy can result in a range of symptoms, depending on which chromosome is affected.