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Gorlin-Goltz syndrome – a medical condition requiring a multidisciplinary approach
Gorlin-Goltz syndrome is a rare genetic condition showing a variable expressiveness. It is inherited in a dominant autosomal way. The strongest characteristic of the disease includes multiple basal cell carcinomas, jaw cysts, palmar and plantar pits, skeletal abnormalities and other developmental de...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
International Scientific Literature, Inc.
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3560657/ https://ncbi.nlm.nih.gov/pubmed/22936202 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.883341 |
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