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A case of myelodysplastic syndrome with abnormal megakaryocytes and ins(8;3)(q24;q21q26)

✍ Scribed by M. Bachy-Delhomme; M.F. Bertheas; J. Jaubert; P. Calmard; C. Vasselon; J. Reynaud; C.P. Brizard

Book ID
119105012
Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
268 KB
Volume
55
Category
Article
ISSN
0165-4608

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A case of atypical myelodysplastic syndrome with micromegakaryocytes, normal platelet count, and t(3;12)(q21;p13) with inv(3)(q21q26)
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A 49-year-old woman patient with atypical myelodysplastic syndrome (MDS) showing a der(3)t(3;12)(q21;p13), and der(12)t(3; 12)(q21;p13)inv(3)(q21q26) as an acquired chromosomal abnormality in the bone marrow is described. The chromosomal breakpoints of the presented complex aberration with combinati