An unbalanced translocation occurs when a chromosome breaks and part of it is transferred to another chromosome, but the sizes of the transferred segments are unequal. This can result in genetic material being duplicated or deleted, leading to a genetic imbalance.
In humans, unbalanced translocations can cause a variety of genetic disorders and health problems. Some common effects of unbalanced translocations include developmental delays, intellectual disabilities, physical abnormalities, and fertility issues. The severity of the effects depends on which chromosomes are involved in the translocation and the specific genes that are affected.
Unbalanced translocations can be inherited from a parent who carries the balanced form of the translocation, or they can occur as a spontaneous mutation. Genetic testing and counseling can help individuals and families understand the implications of an unbalanced translocation and make informed decisions about their healthcare and reproductive options.
Explain how an unbalanced translocation occurs and how it affects humans.
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