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Gorlin-Goltz syndrome
Gorlin-Goltz syndrome is a rare multisystemic disease inherited in an autosomal dominant pattern. It is characterized by numerous basal cell carcinoma of the skin, jaw cysts, and skeletal anomalies such as frontal bossing, vertebral anomalies, palmoplantar pits, and falx cerebri calcification. There...
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| Publicat a: | Turk Pediatri Ars |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Turkish Pediatrics Association
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5644586/ https://ncbi.nlm.nih.gov/pubmed/29062253 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2017.2992 |
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