FIGURE 3: Syndromes categorized by typical course
| Progressive syndromes |
|
| Cockayne | Mucopolysaccharidoses 1 |
| Duchenne muscular dystrophy | Myotonic dystrophy |
| Lowe | Rett syndrome |
| Non-progressive syndromes | |
| Angelman |
Prader-Willi |
| Coffin-Lowry | Rubenstein-Taybi |
| Coffin-Siris | Sex aneuploidies 2 |
| Cornelia de Lange | Smith-Lemli-Opitz |
| Cri du chat | Smith-Magenis |
| Crouzon | Sotos |
| Down's | Tuberous sclerosis |
| Fragile-X | Velocardiofacial |
| Kallman | Williams |
| Neurofibromatosis type 1 | Wolf-Hirschhorn |
| Noonan | |
| Remedial progressive syndromes 3 | |
| Galactosaemia | |
| Phenylketonuria |
1 Lysomal storage disorders (for more detailed information
see O'Brien et al., 2002)
2 Sex aneuplodies include Turner and Klinefelter syndromes
3 Syndromes in which the course can be determined by dietary
intervention