first author

Abstract excerpt

Tatton-Brown-Rahman syndrome (TBRS) is an uncommon overgrowth and neurodevelopmental condition arising from heterozygous mutations in DNMT3A, which confer a predisposition to hematologic cancers. We report a 10-year-old boy diagnosed with classical Hodgkin lymphoma who was subsequently identified to harbour the pathogenic DNMT3A p.Arg882Cys variant. He responded completely to standard ABVD chemotherapy. This obser...

Topics

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• Chromosome Aberrations
• Congenital Abnormalities
• Factor V
• Forecasting
• Genetic Predisposition to Disease
• Herpesvirus Infections and Treatments
• Prothrombin
• Thromboembolism

Identifiers and source

Literature Corpus work

4c2e3a64-91b7-51d1-ac3e-195ddfe68186

DOI

10.22541/au.176051369.93711508/v1