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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...
Autores principales: | Chang, Yi-Lin, Lin, Joseph, Li, Yu-Hsien, Tsao, Lien-Cheng |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190964/ https://www.ncbi.nlm.nih.gov/pubmed/32368543 http://dx.doi.org/10.12998/wjcc.v8.i8.1502 |
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