The discovery may help shed light on how prehistoric societies treated children with rare conditions.
Scientists have diagnosed Down syndrome from DNA in the ancient bones of seven infants, one as old as 5,500 years. Their method, published in the journal Nature Communications, may help researchers learn more about how prehistoric societies treated people with Down syndrome and other rare conditions.
Down syndrome, which occurs in 1 in 700 babies today, is caused by an extra copy of chromosome 21. The extra chromosome makes extra proteins, which can cause a host of changes, including heart defects and learning disabilities.
Scientists have struggled to work out the history of the condition. Today, older mothers are most likely to have a child with the condition. In the past, however, women would have been more likely to die young, which might have made Down syndrome rarer, and the children born with it would have been less likely to survive without the heart surgery and other treatments that extend their lives today.
Archaeologists can identify some rare conditions, such as dwarfism, from bones alone. But Down syndrome — also known as trisomy 21 — is a remarkably variable condition.
Translocation is not referred to as Trisomy 21
Correct, which is why I didn’t use the word “trisomy” when referring to the translocation case. My point is that, even in that situation, the condition is caused by the presence of the translocated piece of chromosome 21 in addition to 2 normal copies. It’s not referred to as a trisomy, as many times only part of the entire chromosome is translocated, but the functional cause of the condition is the same. So, when writing a paper for the general population, it’s not a stretch to call Down Syndrome and Trisomy 21 synonymous.