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Gorlin-Goltz syndrome
Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder, which is characterized by multiple odontogenic Keratocysts and basal cell carcinomas, skeletal, dental, ophthalmic, and neurological abnormalities, intracranial ectopic calcifications of the falx cerebri, and facial dysmorph...
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| Main Authors: | , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Medknow Publications & Media Pvt Ltd
2012
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3283966/ https://ncbi.nlm.nih.gov/pubmed/22363371 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1735-3327.92963 |
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