Anaesthetic management of a patient with Laurence Moon Biedl syndrome undergoing ostium primum atrial septal defect closure

Laurence-Moon-Biedl Syndrome is primarily a rare, recessively inherited genetic disorder. The cardinal features are polydactyly, obesity and retinitis pigmentosa, mental retardation, genital hypoplasia and cardiac anomalies. This spectrum may extend and may also involve renal anomalies. Here, we rep...

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Detalles Bibliográficos
Autores principales: Dhulkhed, Vithal K., Shetti, Akshaya N., Dhulkhed, Pavan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173537/
https://www.ncbi.nlm.nih.gov/pubmed/25885848
http://dx.doi.org/10.4103/0259-1162.118980

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173537/
https://www.ncbi.nlm.nih.gov/pubmed/25885848
http://dx.doi.org/10.4103/0259-1162.118980

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