This is an excellent question. This goes into the field of Biology. I'll try to make this as easy as I can. We all have little things that determine what we are and what we look like. These are called chromosomes. Each chromosome determines what our traits (i.e. eye color, hair color, brow color, etc) will be. Each of us have 46. But when it comes to giving life, men contribute 23 chromosomes to a child while women give the other 23. Our chromosomes are known as X and Y. Women contribute what we call XX Chromosomes. Men Contribute what we call Xx or XY Chromosomes (we'll stick with XY). The Y is what makes males... male. The Y chromosome is also a recessive gene. Now take a look at this chart: .......X.......Y X X Above is what biologists use to help determine the probability (possibility) of a number of outcomes. .......X....... Y X ...XX.......... <------ XX will determine dominant traits (female in this case) X ................. _________________ ......X .......YX ............XY <------ XY will determine Recessive traits (male) X ................ ---- Now that you understand how the table works, let's understand the table with disease. Diseases are passed down, usually, through a recessive gene (Xx or XY) So, if a man or woman has Disease A his/her Genes Look Like this: Xx or xx The people who do not possess this disease have genes like this: XX Those with XX have absolutely no trace of a passed down geneticaly linked disease. Those with Xx are what we call "carriers" because though they may not suffer from the disease, they can still pass it on. Those with xx suffer from the disease. Now, back to our table. Anthony has Xx Nancy has XX ......X .......x X ...XX.... Xx X ...XX ....Xx This table shows that none of their children will have the disease, but they have a 50% chance of being a carrier. John has Xx Mary has Xx .......X....... x X ...XX .....Xx x ... Xx .....xx In this table, John and Mary's children hold a 25% chance of being affected by Disease A, while they hold a 75% chance of being a carrier (those affected count as carriers) and only 25% chance of not being able to pass the disease. Now you know why some children are inherit a passed down family disease.
can not be passed from generation to generation
Haemophilia is a sex-linked recessive disorder - which means it can skip a generation, but only if it is carried in the female line.A female can be a carrier of haemophilia, but a male cannot. This is because males only have one X chromosome, so if they have a defective X they will have the disorder. If a father has haemophilia, all of his daughters will also have haemophilia.
Hereditary diseases are passed down from one generation to the succeeding generation through genes. A lot of research and development has been done to treat it but there is no treatment for this condition.
Hereditary diseases are passed from one generation to another through genetic mutations carried in the DNA of the parent that are passed on to their offspring. These mutations can affect the functioning of specific genes, leading to the development of a hereditary disease in the offspring. This process occurs during fertilization when genetic material is combined from both parents.
Recessive alleles are known for skipping a generation. This is because the phenotype associated with a recessive allele is only expressed when an individual inherits two copies of the recessive allele, one from each parent. If one parent carries the allele but does not exhibit the trait, it can appear to "skip" a generation before being expressed.
can not be passed from generation to generation
The term "genetic disease" refers to a disease that is inherited- or passed from one generation to the next.
While gallbladder disease may have genetic components, it does not keep track of the last generation affected. It can "skip" a generation or affect the children of affected patients.
Yes it can vcaus
diabetes is not passed on
Haemophilia is a sex-linked recessive disorder - which means it can skip a generation, but only if it is carried in the female line.A female can be a carrier of haemophilia, but a male cannot. This is because males only have one X chromosome, so if they have a defective X they will have the disorder. If a father has haemophilia, all of his daughters will also have haemophilia.
yes it can skip a generation, since it is a Mendel inheritance. and it is a reccesive trait. therefore offspring's can have two unaffected parents but chances are both parents might be carriers
If it runs in the family, yes. Some traits skip a generation.
They are caused by abnormal genes and so are passed from one generation to the other on the DNA.
It is possible to have multiple sets of multiples, and giving birth to multiples can also skip a generation. Hyper ovulation (the tendency to release multiple eggs during ovulation, increasing the chances of conceiving fraternal twins) is a factor in giving birth to twins.
http://bulbapedia.bulbagarden.net/wiki/List_of_TM_and_HM_locations got to that link and skip to Generation IV
The person with the recessive trait seems to 'skip' a generation