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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chang, Yi-Lin, Lin, Joseph, Li, Yu-Hsien, Tsao, Lien-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Case Report
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

Internet

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

Ejemplares similares