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Unusual association of Axenfeld-Rieger syndrome and wandering spleen: A case report
BACKGROUND: Axenfeld-Rieger syndrome (ARS) is an autosomal dominant genetic disease characterized by ocular developmental disorders and its association with torsion of wandering spleen (WS) has not been reported to date to the best of our knowledge. This study aimed to describe a rare case of ARS ob...
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| Publicado no: | World J Clin Cases |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7190964/ https://ncbi.nlm.nih.gov/pubmed/32368543 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v8.i8.1502 |
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