Gorlin syndrome: A case report
Gorlin syndrome is a rare autosomal dominant disorder which characterize by multi-organ abnormities such as odontogenic keratocysts in the jaw, skeletal abnormities and multiple basal cell carcinoma etc. We report a case of this syndrome in a young man with palmar pits, multiple facial BCC, clacific...
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| Autores principales: | , , |
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| Formato: | Libro |
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Our Dermatology Online,
2016-01-01T00:00:00Z.
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| Número de Clasificación: |
A1234.567 |
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