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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Detaylı Bibliyografya
Asıl Yazarlar: Singh, Usha Rani, Asif, Shujaath, Kommu, Peter Prasanth Kumar, D’Souza, Philomina
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2012
Konular:
Case Report
Online Erişim: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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