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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2012
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| Matèries: | |
| Accés en línia: | 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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