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Constitutional Mismatch Repair Deficiency Syndrome in a patient from India
Chandramallika Paul1,2, Subhosmito Chakraborty2, Sarit Chakraborty3
1Department of Biochemistry All India Institute of Medical Sciences (AIIMS-Kalyani) Kalyani India.
Abstract:
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 electrophoresis interpretation.
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