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Author

Jigna S. Joshi

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1 paper indexed here

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2026

A Rare t(1;11)(q42;q23) Rearrangement with Trisomy 8 and Trisomy 21 in a Pediatric Acute Myeloid Leukemia Patient with Aberrant CD7 Expression and Jacob Syndrome: Diagnostic Value of Conventional Cytogenetics and Fluorescence in Situ Hybridization in a Rapidly Fatal Case.

This case study shows that AML with a KMT2A gene rearrangement is associated with an aggressive clinical course and uncommon cytogenetics, emphasizing the need to use FISH and cytogenetics together for the detection of gene fusions, partner chromosomes, and other cytogenetic aberrations.

P. Trivedi, Nidhi Patel, Jigna S. Joshi et al. · 0 citations

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