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September 7, 2015Clinical Case ReportsOpen Access

Successful treatment of fetal hemolytic disease due to glucose phosphate isomerase deficiency ( GPI ) using repeated intrauterine transfusions: a case report

P. N. Adama van Scheltema Ai Zhang Lynne M. Ball Sylke J. Steggerda Richard van Wijk Dietje E. Fransen van de Putte Inge L. van Kamp

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Abstract

Hemolytic anemia due to GPI deficiency can be severe and life threatening during fetal life. When parents decline invasive testing, ultrasound monitoring of fetuses at risk is feasible. Intrauterine transfusion can be effective for the treatment of severe fetal anemia due to GPI deficiency.

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Scheltema et al. (2015) studied this question.

synapsesocial.com/papers/6a9fada437a2f8dc0e6183f8 https://doi.org/10.1002/ccr3.358

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1First trimester monitoring of a pregnancy at risk for glucose phosphate isomerase deficiencyOriginal Research · 1986 · 8 citations
2Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.Original Research · 1979 · 41 citations
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