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.
MeSH terms
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Child, Preschool
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Chimera
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Chromosomes, Human, Pair 22 / genetics
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DiGeorge Syndrome / complications*
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DiGeorge Syndrome / genetics
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DiGeorge Syndrome / immunology
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Fatal Outcome
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Female
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Fetomaternal Transfusion / complications*
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Fetomaternal Transfusion / genetics
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Graft vs Host Disease / complications*
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Graft vs Host Disease / immunology
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Humans
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Immunoglobulin G / immunology
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Immunoglobulin M / immunology
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Pedigree
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Pregnancy
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T-Lymphocytes / immunology*
Substances
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Immunoglobulin G
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Immunoglobulin M