No. It arises due to point mutations (like A -> T).
According to the research I've done, Prader-Willi Syndrome is rarely a result of translocation, but it is a possibility. Translocation in this syndrome results in an inactivation of genes on the paternal chromosome 15.
African American and Hispanic are greatly affect by sicklecell.
No
Transfer of genes between nonhomologous chromosomes is known as chromosomal translocation. It can result in the fusion of two chromosomes or the exchange of genetic material between them. This process can lead to genetic abnormalities and diseases.
Translocation
Translocations can result into gene dysregulation, thus leading to diseases like cancer.
This is known as a chromosomal translocation, which can result in genetic material being exchanged between chromosomes. Translocations can lead to disruptions in gene expression and potential genetic disorders. Depending on the specific genes involved, translocations can have diverse effects on an individual's health.
Chromosomal translocation can lead to genetic disorders and cancer. It can result in the fusion of genes from different chromosomes, creating abnormal gene products that may interfere with normal cellular functions. This can disrupt gene expression and lead to the development of various health conditions.
Leaching is another word for translocation.
There is no disease that is the result of hyperthyroidism. Hyperthyroidism is a symptom, not a disease. Hyperthyroidism however, is the result of other disease processes including:Graves' DiseaseHashimoto's thyrotoxicosisIodine toxicityCancer
It can be. Basically most mutations (regardless of type; translocation, reversal, transcription, etc...) can cause hemophilia if they occur within a specific part of the genetic sequencing that codes for the production of the clotting factor proteins. This genetic sequence if found in a segment of the X chromosome.
A disease that you have acquired as a result of the career that you are in.