Angelman syndrome affects both males and females equally. It is a genetic disorder that is not linked to a specific sex chromosome.
Understanding Angelman Syndrome
Angelman syndrome is a rare neurodevelopmental disorder that affects a person's ability to learn, move, and speak. It is caused by a missing or inactive gene on chromosome 15, which is inherited from the mother.
Key Points to Remember:
- Angelman syndrome is not sex-linked, meaning it affects males and females equally.
- The genetic mutation responsible for Angelman syndrome is inherited from the mother.
- While the syndrome affects both genders, it is important to note that the specific symptoms and severity can vary between individuals.
