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(12 baby girl infent is skaryotypically male (XY) is born !o # man and & woman. Later, this diagnosed with Turner"$ like syndronocn determination Ubing In ...

Question

(12 baby girl infent is skaryotypically male (XY) is born !o # man and & woman. Later, this diagnosed with Turner"$ like syndronocn determination Ubing In your knowledge of sex- humans, answer the following questions: Give two genes that might be affected, Give oe mechanism (discussed in class) by which this condition have occurred may Svhat is the usual karyotype observed in individuals who have Syndrome? Turners

(12 baby girl infent is skaryotypically male (XY) is born !o # man and & woman. Later, this diagnosed with Turner"$ like syndronocn determination Ubing In your knowledge of sex- humans, answer the following questions: Give two genes that might be affected, Give oe mechanism (discussed in class) by which this condition have occurred may Svhat is the usual karyotype observed in individuals who have Syndrome? Turners



Answers

A woman with X-linked color blindness and Turner syndrome had a color-blind father and a normal mother. In which of her parents did nondisjunction of the sex chromosomes occur?

All right, so we're given a scenario here where we have to fino typically normal parents, which I've labeled as M for Mother and F for father. They've produced a child who, unfortunately, has a disability. We've been given their chromosomes in order to figure out why this happened, despite the fact that both parents are feeling typically normal African see from the mother's chromosomes, which I've tried to replicate here in the most with the most important information is that she has a chromosome right here that is slightly different than the fathers. And if you look a little bit closer, we can see that the fathers is probably what is normal and the mothers is probably was abnormal, considering they're the chromosomes are of different lengths, and a second chromosome nearby has genetic information that would normally be on this crumb zone. But because it's just a trans location and not a delusion, everything like that, she's feeling typically normal because all the information is still there, right? And so if you look over to this child, we can see that he has a similar short chromosome to the mother. However, in the second pair of chromosomes, there is no extra bit here. Order to make up for the information that was lost on the mother. And so this child has lost some genetic information and is therefore a hypo employed for this information.

Hello there students today, we're going to be answering this question where they want, sorry or they want to know the examination of a kyra type or feels 23 pairs of chromosomes with each home meal? Home dialogue. Just pair illustrating similar size and um central tree. Mm Murray. Sorry, location. Um Which of the following can be concluded from this. Um kyra type. Is it um The individual has down syndrome. The individual is a female individual does not have um cystic fibrosis. Or is it the individual does not have sickle cell anemia? Well, what we brought to see with the okay kyra type and when we use the cara type, cara type is used to um this self to look into cut kind kind of. But I said it right in one video and I'm messing it up Klinefelter syndrome. And it's just basically a genetic condition in which a meal it's born with an extra copy of an X chromosome. And so with that when it comes down to the so that so when it comes down for the kyra type for the kyra type, it just shows a collection of chromosomes. And when we see um for the examination where it fulfils 23 pairs of chromosomes and each has a homie lodges pair. So the paris homie lodges, um it's safe to say based off of um the choices. It seemed to say that the individuals are female and the reason for that. We think about the female chromosome. What do they, what determines the sex of the of the individual or the offspring being a female two X chromosomes? So you have that, is it? I hope you found this helpful. And please feel free to look at the content from other creators that go over and explain whatever checked questions you need extra help with. Okay.

So there are a lot of sex chromosome abnormalities. Eso on a screen here, I show used to be different, most common kind. The 1st 1 is Turner Syndrome of those individual has, um x o Carroll type that mean still why copies lost and those individual yearly are steroid. And they have gross retardation and ah, hard problem and other impairment. Well, obviously, gene on the Y chromosome are lost, and then they call us the most of your issue. Now, with a mirror syndrome Klinefelter syndrome, those individuals have one extra copy of X, so they have X alive. Additional copy of X now for those individuals stayed usually are also sterile because after X copy, but they usually ah have variable degree of um, abnormality. And also they have only very mild and go mental and behavioral problem because obviously, both genes are all the genes are X, and why are there? But they just have some extra X, so the over expression of certain gene can cause issues. So this is also ah, common kind, and there will be a devil. Why seen draw? Those individual has a extra wide copy, and due to the high incidence of work from home loss and those individual our yearly for toe and their ah syndrome or their symptoms are very, very mild There. Sometimes skip went into regular people because, um, they have both x and y and ah um y chromosome has been refuted the little gene and sometimes, you know it doesn't in noticeable if you know, type. Now. There are also some other, more rare abnormalities, like three copy of ex and why or full copy of X Onley. But there is one thing in common we could can never find any individual that has a why ofunato type. That means there's no X chromosome and white only. And this is because what X chromosome contains a lot of housekeeping genes that are essential for the viability of the individual, not just sex determination. Eso the individual without extremism. Kendra survive, period. So, um, so the answer here is de, um, the classrooms, mountain container genes that relate to a sex determination and essential for life? No. And there is another answer E. So obviously Carol type is, uh, the technology actual revealed a genetic abnormality, So we are able to do that to show abnormalities. So the e and also is correct


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