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Updated: Aug 30, 2026

Chromosome Preparation From Cultured Cells
Published on: January 28, 2014
A case of Down syndrome with acute lymphoblastic leukemia and isochromosome Xp
Jillian M Baker1, Max J Coppes, Birgitte Roland
1Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
Abstract:
A 3-year, 9-month-old girl with trisomy 21 was diagnosed with acute lymphoblastic leukemia (ALL). The karyotype of her leukemic cells at diagnosis-48,XX,+i(X)(p10),+21c-included an extra, structurally abnormal X chromosome as the sole acquired abnormality. While an extra X chromosome is a common abnormality in childhood ALL, it is seldom the only acquired aberration. Furthermore, an additional X chromosome that is structurally abnormal is rare, and has not been reported previously as a solitary abnormality. Here we report a novel karyotype in childhood ALL and review the eight previously described cases of ALL with an extra X isochromosome as the only acquired abnormality.
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