High risk of malignancy in mosaic variegated aneuploidy syndrome

S Jacquemont, M Bocéno, JM Rival… - American journal of …, 2002 - Wiley Online Library
S Jacquemont, M Bocéno, JM Rival, F Méchinaud, A David
American journal of medical genetics, 2002Wiley Online Library
Fourteen cases of mosaic variegated aneuploidy (MVA) syndrome have been reported in
the last 10 years. The phenotype of this rare condition has been quite consistent: severe
microcephaly, growth deficiency, mild physical anomalies, and mental retardation. We
describe here a young boy in whom MVA syndrome is associated to myelodysplasia with a
monosomy 7 bone marrow clone. At the age of 3 years, myelodysplasia progressed to an
acute lymphoblastic leukemia, and the patient died soon after. Several syndromes with short …
Abstract
Fourteen cases of mosaic variegated aneuploidy (MVA) syndrome have been reported in the last 10 years. The phenotype of this rare condition has been quite consistent: severe microcephaly, growth deficiency, mild physical anomalies, and mental retardation. We describe here a young boy in whom MVA syndrome is associated to myelodysplasia with a monosomy 7 bone marrow clone. At the age of 3 years, myelodysplasia progressed to an acute lymphoblastic leukemia, and the patient died soon after. Several syndromes with short stature and severe microcephaly, such as the Seckel and Nijmegen syndromes, comprise hematological findings and chromosome instability. However, chromosome instability was not comfirmed in our patient. MVA with hematological findings has not been reported before, but 3 patients of 14 (21%) have developed a malignancy (rhabdomyosarcoma, acute lymphoblastic leukemia, and nephroblastoma). Therefore, we propose that MVA is a condition predisposing to neoplasia. © 2002 Wiley‐Liss, Inc.
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