Answer:
The correct answer is: Fragile X Syndrome.
Step-by-step explanation:
Fragile X Syndrome is a genetic condition that has an X-linked dominant inheritance, which means that this disorder is carried in a gene in the X chromosome (23rd pair) and will affect any child with one allele.
Given that males only get one X chromosome, while females get two, this condition tends to affect males on a deeper level.
People with Fragile X Syndrome suffer from intellectual disability (the average IQ in males is under 55), characteristic physical features such as a long and narrow face, big protruding ears, flexible fingers and large testicles. Autism and hyperactivity are also common.