Well there is actually several. There is XXY, Klinefelter: XYY, "Super male": XXX, perfectly normal but still a abnormality: and XO or Turner syndrome, sterile female, small stature, normal intelligence. These are the most well documented but I am sure there is more out there.
Downsyndrome
There are many different chromosomal abnormalities in a RETT patient it includes ring chromosome(especially X chromosome),dicentric,chromosomal and chromatid breaks etc...
The Philadelphia chromosome abnormality is that chromosome 9 and 22 have swapped places. This abnormality causes a higher susceptibility to forms of leukemia. Specificly it is connected most commonly to chronic myelogenous leukemia.
Trisomy 21, Down's syndrome
Mirroring chromosomes are a genetic abnormality. This abnormality is caused by an exact duplication of a chromosome segment, including the centromere.
In humans, which sex chromosome determines if an offspring is a male or female?
There are many different chromosomal abnormalities in a RETT patient it includes ring chromosome(especially X chromosome),dicentric,chromosomal and chromatid breaks etc...
Yes, it takes place in chromosome 4.
yes it is. It affects chromosome 11.
A chromosomal abnormality occurs when any of the genes that make up a human, animal, or plant has a genetic mutation.
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.
what is the answer to this question
Chromosomal abnormality is a broader term, describing duplications, loss, gain etc, of a particular chromosome. More related to the structures in an ideogram.Genetic disorder is a much broader term that describes any chromosomal or genetic changes. A disease condition.
Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
Yes it is, the mutation lies on chromosome 15. This carries the code for the structure of fibrillin which is an important part of collagen, the main component of connective tissue.
A abnormality in the size, shape, or number of chromosomes.
Trisomy an abnormality in chromosomal development.
By what is called as amniocentesis, you can diagnose the chromosomal abnormality of the unborn baby. You do this procedure under cover of ultrasonography. The fetal cells will give you complete picture of the chromosomal abnormality of the unborn child.