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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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| 出版年: | Turk Pediatri Ars |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Turkish Pediatrics Association
2017
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| 主題: | |
| オンライン･アクセス: | 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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