A Trisomy 1. Another said this was Down's Syndrome.
No, not all cases of Down syndrome involve a complete extra chromosome. The most common form, known as trisomy 21, consists of an entire extra chromosome 21, resulting in three copies instead of the usual two. However, some cases are due to a Robertsonian translocation, where a part of chromosome 21 is attached to another chromosome, or mosaic Down syndrome, where some cells have the extra chromosome while others do not.
Meiotic nondisjunction. In meiosis I or II, chromosome pair 21 fail to separate correctly, leaving one gamete with an extra chromosome 21.
A boy has one X chromosome from the mother and one Y chromosome from the father, making his chromosome pair for gender determination XY.
its usually the size of it and the information that is in the pair
If someone has an extra chromosome it means there was a genetic mutation that is abnormal in human development. It may result in problems with the person affecting them on a basic level, or may go fully unnoticed. A common disorder that can be caused by having an extra chromosome is Down's Syndrome.
no, an extra copy of chromosone 21 causes down syndrome
In a trisomy syndrome, an extra chromosome is present so that the individual has three of a particular chromosome instead of the normal pair.
Down syndrome
It is most commonly caused by increased maternal age.Add: It is the result of nondisjunction of the 21st chromosome pair, in which the pair fails to separate, so that one cell gets an extra copy of chromosome 21.
No, not all cases of Down syndrome involve a complete extra chromosome. The most common form, known as trisomy 21, consists of an entire extra chromosome 21, resulting in three copies instead of the usual two. However, some cases are due to a Robertsonian translocation, where a part of chromosome 21 is attached to another chromosome, or mosaic Down syndrome, where some cells have the extra chromosome while others do not.
Meiotic nondisjunction. In meiosis I or II, chromosome pair 21 fail to separate correctly, leaving one gamete with an extra chromosome 21.
It is the result of a chromosomal abnormality, in which there is an extra chromsome on the chromosome 21 pair. This is call trisomy 21.
A boy has one X chromosome from the mother and one Y chromosome from the father, making his chromosome pair for gender determination XY.
in Patau there is an extra chromosome in chromosome 13, in Edwars it the extra chromosome is in chromosome 18
translocation
its usually the size of it and the information that is in the pair
Aneuploid - the individual has an extra copy of one chromosome or is missing a chromosome.