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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 28/04/07 |
| Symbol | ISCC |
| Location | 7p21.1 |
| Name | isolated sagittal or coronal synostosis |
| Corresponding gene | TWIST1 |
| Main clinical features | premature fusion of one or more cranial sutures |
| Genetic determination | not applicable |
| Prevalence | 1 in 2,500 live births |
| Function/system disorder | osteo-articular |
| Type | malformation |
| Remark(s) |