Cockayne syndrome–xeroderma pigmentosum complex with demyelination: A rare association

Xeroderma pigmentosum–Cockayne syndrome (XP–CS) includes facial freckling and early skin cancers typical of XP and some features typical of CS, such as mental retardation, spasticity, short stature, and hypogonadism. XP–CS does not include skeletal involvement, the facial phenotype of CS, or CNS dem...

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Detalles Bibliográficos
Autores principales: Singh, Usha Rani, Asif, Shujaath, Kommu, Peter Prasanth Kumar, D’Souza, Philomina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385169/
https://www.ncbi.nlm.nih.gov/pubmed/22754238
http://dx.doi.org/10.4103/0971-6866.96681

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385169/
https://www.ncbi.nlm.nih.gov/pubmed/22754238
http://dx.doi.org/10.4103/0971-6866.96681

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