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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) |