Gorlin-Goltz Syndrome: Diagnosis and Treatment Options
The Gorlin-Goltz syndrome is a rare autosomal dominant hereditary condition, with complete penetrance and variable expressivity. Characterized by the appearance of multiple basaliomas, and often the development of keratocyst, it can also express itself by the presence of palmar/plantar depressions,...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Ordem dos Médicos
2017-05-01
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| Series: | Acta Médica Portuguesa |
| Subjects: | |
| Online Access: | http://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/7521 |