A Case Report of Gorlin-goltz Syndrome
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in patched (PTCH), a tumor suppressor gene that has been mapped to chromosome 9q22.3-q31. Gorlin-goltz synd...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nab'a Al-Hayat Foundation for Medical Sciences and Health Care - Press
2016-04-01
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| Series: | Journal of Contemporary Medical Sciences |
| Subjects: | |
| Online Access: | http://jocms.org/index.php/jcms/article/view/65 |