Need for preventive diagnostics in patients with family history of Gorlin-Goltz syndrome (GGS)
Background: Gorlin-Goltz syndrome is a disease develops as a result of genes PTCH1, PTCH2 or SUFU mutations which increases the risk of neoplasms. Craniofacial anomalies constitute the majority of the typical features of the disease. Case: The authors describe the case of a 68-year-old patient refer...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2022-04-01
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| Series: | Advances in Oral and Maxillofacial Surgery |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2667147622000164 |