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Gorlin-Goltz syndrome in twin brothers: an unusual occurrence with review of the literature
Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is caused by genetic alteration produced by a mutation in the ‘patched’ tumour suppressor gene, and is inherited in a dominant autosomal way. Although sporadic cases have been found, this syndrome has rarely been reported in...
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| Gepubliceerd in: | BMJ Case Rep |
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| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMJ Publishing Group
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4551002/ https://ncbi.nlm.nih.gov/pubmed/26297769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-211608 |
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