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...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Elsevier,
2022-04-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |