Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
http://www.nature.com/articles/7211657.pdf
Reference17 articles.
1. Castillo RA, Devoe LD, Hadi HA, Martin S, Geist D . Nonimmune hydrops fetalis: clinical experience and factors related to a poor outcome. Am J Obstet Gynecol 1986; 155: 812–816.
2. Jones DC . Non immune fetal hydrops: diagnosis and obstetrical management. Semin Perinatol 1995; 19: 447–461.
3. Whitfield CF, Follweiler JB, Morrow LL, Miller BA . Deficiency of α-spectrin synthesis in burst forming units – erythroid in lethal hereditary spherocytosis. Blood 1991; 78: 3043–3051.
4. Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N et al. Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. J Clin Invest 1997; 99: 267–277.
5. Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL et al. Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene. J Clin Invest 1995; 95: 1174–1182.
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