A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited

De Barsy syndrome (DBS), synonymously known as autosomal recessive cutis laxa type III, is an extremely rare condition clinically characterized by cutis laxa, a progeroid appearance, and ophthalmologic abnormalities. We present here an account of 5-year follow-up since the birth of an Indian boy wit...

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Detalles Bibliográficos
Autores principales: Dutta, Abhijit, Ghosh, Sudip Kumar, Ghosh, Arghyaprasun, Roy, Sutirtha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763701/
https://www.ncbi.nlm.nih.gov/pubmed/26955101
http://dx.doi.org/10.4103/0019-5154.174031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763701/
https://www.ncbi.nlm.nih.gov/pubmed/26955101
http://dx.doi.org/10.4103/0019-5154.174031

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