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What else can I help you with?
What are the scenarios of passing turner syndrome?
Turner syndrome is a genetic condition that affects females, typically resulting in short stature, delayed puberty, and infertility. Some individuals may also experience heart defects, kidney abnormalities, and learning disabilities. Although it is a lifelong condition, many individuals with Turner syndrome lead healthy and fulfilling lives with medical monitoring and support.
What is the inheritance of marfan syndrome is an example of?
The inheritance of Marfan syndrome is an example of an autosomal dominant genetic disorder. This means that a person only needs to inherit one copy of the mutated gene from one parent in order to develop the condition.
Is apert syndrome dominant or recessive?
Apert syndrome is typically caused by a sporadic mutation in the FGFR2 gene and is not inherited in a simple dominant or recessive manner. It is considered an autosomal dominant condition, with most cases arising from new mutations.
How does a person inherit Goldenhar Syndrome?
Goldenhar syndrome is not an inherited syndrome, it is just in a persons genes and there is no way to stop a baby from getting it in the womb. Goldenhar syndrome is not developed or passed on to the foetus it is just there. hope this helped you as i am a sufferer of goldenhar syndrome myself! :)
What causes disorders such as klinefelter syndrome and turner syndrome?
Klinefelter syndrome is a chromosomal condition that only affects males and is characterized by a male having an additional X chromosome (XXY) in cells. This chromosome abnormality occurs when there is an error in cell division, resulting in an extra copy of the X chromosome.
Is turner syndrome inheritable or random?
Turner syndrome is usually random and not inherited. It occurs when a female is born with a missing or incomplete X chromosome. In rare cases, Turner syndrome can be inherited if one parent carries a chromosomal abnormality.
What are the scenarios of passing turner syndrome?
Turner syndrome is a genetic condition that affects females, typically resulting in short stature, delayed puberty, and infertility. Some individuals may also experience heart defects, kidney abnormalities, and learning disabilities. Although it is a lifelong condition, many individuals with Turner syndrome lead healthy and fulfilling lives with medical monitoring and support.
What are causes of Marfan syndrome?
It is a genetic disorder and if one parent has it, there is a 50?50 chance that the child will have it.
How do you get Apert syndrome?
Apert syndrome is a genetic defect, so that means that the child will have it from conception (it's an autosomal dominant genetic defect, which means that only one parent needs to supply the defective gene in order for the child to be born with it.)
Could a parent with Down syndrome give their offspring Down syndrome?
As the disease is genetic, DS women have nearly a 50% chance of passing on DS to their offspring if the father does not have DS.
Is there a way to avoid transferring Morquio's syndrome from parent to child?
There is no way to be absolutely positive that your child will not have Morquio's syndrome if both parents have the gene, but there are genetic screenings to help prevent having a child with Morquio's syndrome.
What is responsible for carrying the genetic material of parent cells to new cells?
The DNA molecule is responsible for carrying the genetic material of parent cells to new cells. DNA contains the instructions for building and maintaining an organism, and it is passed down from parent cells to new cells during cell division.
Is apert syndrome autosomal or sexlinked?
Apert syndrome is a autosomal dominant genetic disorder, meaning that only one copy of the mutated gene from either parent is necessary to inherit the condition. It is not sex-linked.
What process is responsible for getting genetic information from parent organism to offspring?
GENES follow me on Instagram lol @FerniBear94
Why do people get down syndrome is it purely genetic?
Down syndrome is purely genetic. There are no known environmental causes of the disorder. It is not a disease that is passed from parent to child. It is simply an disorder when the chromosomes split during cell division during development. The mayoclinic describes the causes: http://www.mayoclinic.com/health/down-syndrome/DS00182/DSECTION=causes
What is UPD?
UPD stands for "uniparental disomy," a genetic condition where an individual inherits two copies of a chromosome from one parent and no copies from the other parent. This can lead to various genetic disorders or developmental issues, depending on which chromosome is affected. UPD can result in abnormal gene expression and can be associated with conditions such as Prader-Willi syndrome and Angelman syndrome, depending on the specific chromosomes involved.
Has anyone fathered a child who has got klinefelter syndrome?
Yes, Klinefelter syndrome typically results from a genetic anomaly involving an extra X chromosome in males, leading to the condition (47,XXY). It is not inherited from a parent in a direct sense, as it usually occurs due to random errors during the formation of sperm or egg cells. Therefore, a father can have a child with Klinefelter syndrome due to such genetic variations, but it is not a hereditary condition passed down from parent to child.
