It is a mutation of cross linked genes in which during separation of haploid cells carries an extra set of information which can cause multiple outcomes, xxy xyy xxx where one is common, one has a 50% survival rate and one has been documented to only have less than 1% survival rate.
Current research on XYY syndrome is focused on understanding the link between the extra Y chromosome and the associated physical and behavioral characteristics of individuals with the condition. Studies are also exploring potential treatments and interventions to address the challenges that individuals with XYY syndrome may face, such as learning difficulties and behavioral issues. Additionally, research is investigating the genetic mechanisms underlying XYY syndrome to improve diagnosis and management of the condition.
by some person
XYY Syndrome
There are seven possible genetic sexes: XX = female XY = male X = female with Turner syndrome XXX = female with X-trisomy XXY = intersex with Klinefelter syndrome XYY = male with 47,XYY syndrome XXYY = male with 48,XXYY syndrome
Down syndrome IS the diagnosis.
You would have 47 chromosomes because you would have the normal 46 but one extra y with the sex determing pair of chromosomes which would make you have super male syndrome.
Yes, Klinefelter's syndrome is due to the XXY genotype.
Jacobs syndrome, also known as XYY syndrome, affects males. It is a genetic condition caused by the presence of an extra Y chromosome in males.
XYY syndrome is caused by an extra Y chromosome in males. This condition typically occurs due to a random error in cell division during either the formation of the sperm or the egg. It is not inherited and does not have a clear genetic cause.
The discovery of the 47 XYY syndrome was first reported by Patricia A. Jacobs and J.A. Strong in 1961. They described a male with an extra Y chromosome, leading to the identification of this chromosomal abnormality.
The diagnosis remains uncertain because of the mildness of the patient's symptoms, the absence of a family history of the syndrome, and other variables. These borderline conditions are sometimes referred to as marfanoid syndromes.
A diagnosis of Marfan syndrome is typically made through a physical exam, family history assessment, and genetic testing. The diagnostic process may also involve imaging tests such as echocardiography and eye examinations to check for Marfan-related complications. Consulting with a medical geneticist or specialist experienced in diagnosing Marfan syndrome is important for accurate diagnosis and management.