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What else can I help you with?
Does TaySachs disease have a dominant or a recessive trait?
recessive
What is a genetic disorder that cannot be detected by karyotyping?
Karyotyping looks at the complete set of chromosomes. It can detect large-scale abnormalities, such as missing/extra chromosomes or whether large pieces of chromosomes have been rearranged. It cannot detect any of the many, many genetic disorders which are caused by a single gene, several genes or gene interactions. Examples of these would be cystic fibrosis, sickle-cell disease and dwarfism.
How is Cerebrovascular disease detected?
Cerebrovascular disease can be detected with a complete neurological examination and specialized imaging technology
Can all genetic diseases be identified in a karyotype?
The can be analyzed to determine the sex of the individual and whether there are any chromosomal abnormalities.
What year was lyme disease detected?
1981
What do you do with an upside down goldfish?
An upside down goldfish means it has a swim bladder disease. If that disease is detected on your goldfish early, it is treatable with isolation and medicated food. But if the disease is detected too late, the results are irreversible-it is a deadly disease.
Is diabetes a curable disease if detected in early?
No. It is at present uncurable.
What would enable you to detect aneuploidy?
Aneuploidy can be detected through various laboratory tests such as karyotyping, fluorescence in situ hybridization (FISH), or chromosomal microarray analysis. These tests analyze the number and structure of chromosomes in a sample of cells to identify any abnormalities. Additionally, non-invasive prenatal testing (NIPT) can be performed on maternal blood to screen for aneuploidies in a developing fetus.
What is the survival rate of a mesothelioma patient?
Well, unfortunately, this relies on numerous factors. One of these factors is when the disease was first detected. If the disease was detected early, as in first 10 years, the patient has a higher survival rate as compared to someone that had it detected after 40 or 50 years of its growth.
What is an example of karyotyping?
Karyotyping is a laboratory technique used to visualize an individual's chromosomes. An example of karyotyping is when a karyotype is created from a blood sample to determine if a person has a chromosomal abnormality, such as Down syndrome, by analyzing the size, number, and shape of their chromosomes.
Why human red blood cells are not suitable for karyotyping?
The karyotype is the number and appearance of chromosomes in the nucleus of a cell. Mature red blood cells don't have a nucleus, so they cannot be used for karyotyping.
Which type of cell could not be used for karyotyping?
Red blood cells (erythrocytes) cannot be used for karyotyping as they do not contain a nucleus. Karyotyping involves examining the number and structure of chromosomes within the nucleus of a cell, which red blood cells lack.
