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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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Bibliografski detalji
Glavni autori: Singh, Usha Rani, Asif, Shujaath, Kommu, Peter Prasanth Kumar, D’Souza, Philomina
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications & Media Pvt Ltd 2012
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3385169/
https://ncbi.nlm.nih.gov/pubmed/22754238
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.96681
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