first author

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 Ho

Authors

Manas Kalra (ORCID: https://orcid.org/0000-0003-2570-7750)
Sunita Bijarnia‐Mahay (ORCID: https://orcid.org/0000-0002-5255-8212)
Shreyasi Das (ORCID: https://orcid.org/0009-0002-4011-5112)

Publication Details

Published: 2025-10-15
DOI: https://doi.org/10.22541/au.176051369.93711508/v1
Primary Topic: Neurogenetic and Muscular Disorders Research
Type: article
Field-Weighted Citation Impact: 0.00

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article

first author

Manas Kalra, Sunita Bijarnia‐Mahay, Shreyasi Das

Oct 15, 2025

Neurogenetic and Muscular Disorders Research

article

first author

Manas Kalra, Sunita Bijarnia‐Mahay, Shreyasi Das

October 15, 2025article en

Abstract

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 Ho

Openalex Percentile: Top 60%

Neurogenetic and Muscular Disorders Research

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first author — Manas Kalra, Sunita Bijarnia‐Mahay, et al. · (2025) | TGRS Research Map | TGRS