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Constitutional Mismatch Repair Deficiency Syndrome in a patient from India
This report highlights an extremely rare genetic condition constitutional mismatch repair deficiency (CMMRD) in an Indian pediatric patient with dual malignancies, who suffered from transient encephalopathy, a rare side effect of the drug Nivolumab and the associated challenge during CSF protein ele...
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| Publicat a: | Clin Case Rep |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7752390/ https://ncbi.nlm.nih.gov/pubmed/33363830 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3249 |
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