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What does the karyotype of a person with turners syndrome look like?
Wiki User
∙ 12y ago
There are a few types of Turner syndrome. The most common two are:
1) Classic - The karyotype is 45X. The second X chromosome in missing from all cells.
2) Mosaic - The karotype is 45X/46XX. The second X chromosome is missing from some cells.
3) There are other types of Turner syndrome in which the second X is only partly missing or it is partly damaged.
Wiki User
∙ 13y ago
Wiki User
∙ 14y agoA person with Turner Syndrome only has an X chromossome (instead of having 2 or one X and a Y). Usually, the missing X is the parental chromossome.
Wiki User
∙ 12y agoYou will see, most generally, three 21 chromosomes. This is why this condition is also called trisomy 21. Normally disjunction provides us with pairs of chromosomes.
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What can be determined from a karyotype?
Analysis of a karyotype determine how many chromosomes are in blood cells. It also determines if there are any missing or extra chromosomal material that are indicators of genetic disorders such as downs syndrome.
What does it tell you about a person if you examine a human karyotype and it looks like there are two x chromosomes?
It means they are female.
If you are a girl and you have turner syndrome when will your growthplates close in your feet?
That would be different for every person with Turner syndrome, just like it would be different for every person without Turner syndrome.
How does a normal karyotype looks like?
Two straight lines
What is the karyotype of ALS?
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that does not have a specific karyotype. ALS can be caused by various genetic mutations, including mutations in genes like C9orf72, SOD1, TARDBP, and FUS. These mutations can be identified through genetic testing, but there is no single karyotype that can definitively diagnose ALS.
What can be determined from a karyotype?
Analysis of a karyotype determine how many chromosomes are in blood cells. It also determines if there are any missing or extra chromosomal material that are indicators of genetic disorders such as downs syndrome.
What does it tell you about a person if you examine a human karyotype and it looks like there are two x chromosomes?
It means they are female.
What would trisomy 21 look like in a karyotype?
The trisomy 21 in a karyotype would look like extra chromosome 21 I ^^
If you are a girl and you have turner syndrome when will your growthplates close in your feet?
That would be different for every person with Turner syndrome, just like it would be different for every person without Turner syndrome.
Can a karyotype determine eye color?
A karyotype is chart that shows all the chormosomes paired up and in order. A karyotype cannot determine eye color but it can determine what colors that specific person carries and can pass down to the next generation. BUT to determine what the next generation eye color will look like, it is not possible yet, but you can do a punnett square and that will show you the possible choice(s).
How does a normal karyotype looks like?
Two straight lines
What are symptoms or effects of turners syndrom?
i fell like jacking off
How can you tell the sex of a person by looking at that person karyotype?
A male would have an X chromosome that literally looks like an X and Y chromosome that still resembles a X but is smaller like a lowercase x. A female would have two X chromosomes
What is is Michael turners 40 yard dash?
it was like about a 4.49, my educated guess.
What is an inherited disease?
An inherited disease is one the other person is passed on to you, like anemia or Down's syndrome.
What is observed in a karyotype?
A karyotype is basically a chart of the number and structure of chromosomes. They can reveal ploidy differences (missing or additional chromosomes such as trisomy 21) or chromosomal mutations (like inversions, deletions, translocations etc)
What is the karyotype of ALS?
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that does not have a specific karyotype. ALS can be caused by various genetic mutations, including mutations in genes like C9orf72, SOD1, TARDBP, and FUS. These mutations can be identified through genetic testing, but there is no single karyotype that can definitively diagnose ALS.
