EDWARDS SYNDROME – SCI & TECH

News: Down syndrome, Edwards syndrome found in ancient individuals

 

What's in the news?

       Researchers have reported chromosomal disorders discovered from prehistoric skeletal remains, dating up to approximately 5,500 years old — including six cases of Down syndrome and one case of Edwards syndrome.

 

Key takeaways:

       According to the authors of a paper published in the journal Nature Communications, the findings may represent the first time Edwards syndrome has been identified from historic or prehistoric remains.

 

Edwards Syndrome:

       It is also known as trisomy 18.

       It is an autosomal chromosomal disorder due to an extra copy of chromosome 18.

       It is a very severe genetic condition that affects child’s body development and growth.

 

Symptoms:

       Children diagnosed with trisomy 18 have a low birth weight, multiple birth defects and defining physical characteristics.

 

Types of Edwards Syndrome:

There are three types of Edwards syndrome such as

 

Complete Trisomy 18:

       It is the most common form (94%).

       In this type, every cell contains three complete copies of chromosome 18.

       The extra chromosome is most often of maternal origin.

 

Mosaic Trisomy 18:

       It is the second most common type (less than 5%).

       In this type, both a complete trisomy 18 and a normal cell line exist.

 

Partial Trisomy 18:

       In this type, only a partial segment of chromosome 18 is present in triplicate.

       The partial triplicate often results from a balanced translocation or inversion carried by one of the parents.

 

Treatment:

       There are no specific treatments for trisomy 18.

       Treatment will focus on the symptoms of the condition, such as heart conditions, breathing difficulties and infections.