Prader-Willi syndrome
Prader-Willi syndrome results from deletion of genetic material from the chromosome 15 inherited of paternal origin, and is a classic example of imprinting.
Typical features include:-
Typical features include:-
- Hyperphagia (excessive eating) and obesity
- Short stature
- Delayed puberty, hypogonadism, infertility
- Learning difficulties
- Compulsive behaviour (e.g. skin picking)
