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Axenfeld–Rieger Syndrome: Rare Case Presentation and Overview
Axenfeld–Rieger syndrome (ARS) is an extremely rare autosomal dominant disorder characterized by ocular, craniofacial, dental and periumbilical abnormalities. We present a case of a 10-year-old boy. Its awareness among oral surgeons is essential for timely diagnosis and subsequent prevention of opht...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Maxillofac Oral Surg |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Springer India
2019
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7410934/ https://ncbi.nlm.nih.gov/pubmed/32801529 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12663-019-01307-9 |
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