https://www.joraldiagnosis.com/revista/article/view/177
Familial case of Gorlin-Goltz syndrome associated with craniosynostosis | Journal of Oral Diagnosis
Gorlin-Goltz Syndrome is inherited as an autosomal dominant disorder and occurs due to mutations in the PTCH1 (Patched 1) gene. It is characterized by multiple...
goltz syndromeassociated withoral diagnosisfamilialcase