Final answer:
Trisomy X does not typically cause phenotypic abnormalities due to X inactivation, a process where one X chromosome in each cell of a female embryo is inactivated, compensating for the extra X chromosome.
Step-by-step explanation:
Trisomy X typically does not cause phenotypic abnormalities because of a process called X inactivation. During early development, one X chromosome in each cell of a female mammalian embryo inactivates by condensing into a structure called a Barr body. The genes on the inactive X chromosome are not expressed. By this process, females compensate for their double genetic dose of X chromosome, which explains why trisomy X does not typically result in significant phenotypic abnormalities.