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Transient myeloproliferative disorder in a phenotypically normal infant with i(21q) mosaicism
Shi-Qi Wu1, Kwan Tien Loh, Xiao-Rong Chen
1Division of Medical Genetics, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. swu@chla.usc.edu
Cancer Genetics and Cytogenetics
|September 19, 2002
Abstract:
We report a case of transient myeloproliferative disorder (TMD) that occurred in a phenotypically normal infant with low level constitutional mosaicism of i(21q). To the best of our knowledge, this is the first documented case of TMD with constitutional i(21q) mosaicism.