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What are examples of genetic disorders that is caused by insertion of extra codons in the x sex chromosome?
The phenomenon of having an extra chromsome is called anueploidy. Depending on the chromosome of which the extra copy exists, there are many disorders.
Down Snydrome is the most common disorder associated with an extra autosomal chromosome, but it is not the only one. The other condintions that come from extra copies of an autosome (non-sex chromosome) that result in the most live births are:
- Edward's Syndrome from an extra copy of 18 and
- Patau syndrome which is caused by an extra 13.
As for sex chromosomes,
- an extra X chromosome results in Klinefelter's syndrome (XXY) in males and
- metafemale or XXX syndrome in women.
- Males with an extra Y are simply refered to as having XYY syndrome.
What else can I help you with?
What is an examples of a genetic disorder that is cause by insertion of extra codons in the X sex chromosome?
Fragile X Syndrome
Why can females but not males be carriers of sex linked genetic disorders?
Females have two X chromosomes, allowing them to be carriers of sex-linked genetic disorders on one X chromosome while having a normal allele on the other X chromosome. Males have only one X chromosome and one Y chromosome, so any genetic disorder on their single X chromosome will manifest as the disorder rather than being masked.
What is an example of a genetic disorder that is caused by insertion of extra codons of the X sex chromosome?
Fragile X Syndrome
What can too few of a type of chromosome cause?
Too few of a type of chromosome can cause genetic disorders or death. Turner Syndrome occurs when there is a missing X chromosome.
What does deletion chromosome consists of?
A deletion chromosome consists of a section of DNA that is missing or deleted from a chromosome. This deletion can result in the loss of specific genes or genetic material, potentially leading to genetic disorders or birth defects. Deletion chromosomes can arise spontaneously or be inherited.
What is an examples of a genetic disorder that is cause by insertion of extra codons in the X sex chromosome?
Fragile X Syndrome
Why can females but not males be carriers of sex linked genetic disorders?
Females have two X chromosomes, allowing them to be carriers of sex-linked genetic disorders on one X chromosome while having a normal allele on the other X chromosome. Males have only one X chromosome and one Y chromosome, so any genetic disorder on their single X chromosome will manifest as the disorder rather than being masked.
What is the significance of Olivia Farnsworth's chromosome 6 deletion in understanding genetic disorders and potential medical advancements?
Olivia Farnsworth's chromosome 6 deletion is significant because it helps researchers understand how genetic disorders can be caused by specific genetic mutations. By studying her case, scientists can gain insights into the role of chromosome 6 in human health and potentially develop new treatments or interventions for genetic disorders linked to this chromosome. This research could lead to advancements in personalized medicine and targeted therapies for individuals with similar genetic conditions.
How can genetic counselors predict genetic disorders?
Well certain disorders are found on certain chromosomes and on certain parts of the chromosome. How they find out how, i don't know. But if some pieces of a specific chromosome they can predict they will have a certain disorder
What does a match on the X chromosome signify in genetic testing?
A match on the X chromosome in genetic testing indicates a shared genetic trait or similarity between individuals, which can be used to trace ancestry or identify potential genetic disorders.
What is an example of a genetic disorder that is caused by insertion of extra codons in the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of an extra codons in the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of extra codons of the X sex chromosome?
Fragile X Syndrome
What is an example of a genetic disorder that is caused by insertion of extra codons in x sex chromosome?
Fragile X Syndrome
What is a change or error in the structure of a gene or chromosome?
A change in the structure of a gene or chromosome is called a mutation. Mutations can occur through different mechanisms such as substitution, deletion, insertion, or rearrangement of DNA sequences, leading to alterations in the genetic information carried by the affected gene or chromosome. Mutations can have various effects on an organism, ranging from no noticeable impact to causing genetic disorders or diseases.
What is chromosome deletion?
u fool give me the answer
What can too few of a type of chromosome cause?
Too few of a type of chromosome can cause genetic disorders or death. Turner Syndrome occurs when there is a missing X chromosome.
