| Literature DB >> 10906029 |
J G Ocejo-Vinyals1, M J Lozano, P Sánchez-Velasco, J Escribano de Diego, J E Paz-Miguel, F Leyva-Cobián.
Abstract
We describe a girl with DiGeorge anomaly and normal cytogenetic and molecular studies, whose clinical course was complicated by graft versus host disease caused by intrauterine materno-fetal transfusion, and several immunohematological alterations including a monoclonal gammapathy of undetermined significance (first IgG, which subsequently changed to IgM). The main clinical features and pathological findings are discussed.Entities:
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Year: 2000 PMID: 10906029 PMCID: PMC1718418 DOI: 10.1136/adc.83.2.165
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791