Abstract
Hereditary xerocytosis is a rare hemolytic anemia occurring secondary to a defect in cell membrane potassium flux. We report a case of severe fetal anemia and non-immune hydrops secondary to hereditary xerocytosis that was managed successfully with in utero erythrocyte and albumin transfusion.
MeSH terms
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Adult
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Amniocentesis
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Anemia, Hemolytic / complications
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Anemia, Hemolytic / genetics
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Anemia, Hemolytic / therapy*
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Blood Transfusion, Intrauterine*
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Cordocentesis
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Erythrocyte Transfusion*
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Female
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Fetal Diseases / therapy*
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Gestational Age
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Humans
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Hydrops Fetalis / etiology*
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Hydrops Fetalis / therapy
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Pregnancy
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Serum Albumin / therapeutic use