Literature DB >> 8822334

Hematologic disorders and nonimmune hydrops fetalis.

M O Arcasoy1, P G Gallagher.   

Abstract

Hematologic disorders are implicated in approximately 10% to 27% of cases of nonimmune hydrops fetalis. In almost all of these disorders, anemia leading to heart failure, edema, ascites, and anasarca is the final common denominator. The etiology of the anemia in these cases can be conveniently divided into two categories: (1) excessive erythrocyte loss by hemolysis or hemorrhage, and (2) erythrocyte underproduction. The former include intrinsic erythrocyte abnormalities such as alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency, and conditions with excessive fetal blood loss such as fetomaternal hemorrhage and twin-twin transfusion. The latter include bone marrow replacement syndromes and conditions associated with failure of erythrocyte production. The presentation, diagnosis, and management of hematologic disorders associated with nonimmune hydrops fetalis are reviewed.

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Year:  1995        PMID: 8822334     DOI: 10.1016/s0146-0005(05)80057-6

Source DB:  PubMed          Journal:  Semin Perinatol        ISSN: 0146-0005            Impact factor:   3.300


  7 in total

Review 1.  Hydrops fetalis caused by homozygous alpha-thalassemia and Rh antigen alloimmunization: report of a survivor and literature review.

Authors:  Divya-Devi Joshi; H James Nickerson; Michael J McManus
Journal:  Clin Med Res       Date:  2004-11

Review 2.  A system-based approach to the genetic etiologies of non-immune hydrops fetalis.

Authors:  Anne H Mardy; Shilpa P Chetty; Mary E Norton; Teresa N Sparks
Journal:  Prenat Diagn       Date:  2019-06-26       Impact factor: 3.050

3.  Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.

Authors:  P G Gallagher; M J Petruzzi; S A Weed; Z Zhang; S L Marchesi; N Mohandas; J S Morrow; B G Forget
Journal:  J Clin Invest       Date:  1997-01-15       Impact factor: 14.808

4.  Hereditary spherocytosis: evaluation of 68 children.

Authors:  Çapan Konca; Murat Söker; Mehmet Ali Taş; Ruken Yıldırım
Journal:  Indian J Hematol Blood Transfus       Date:  2014-04-11       Impact factor: 0.900

Review 5.  Alpha-thalassaemia.

Authors:  Cornelis L Harteveld; Douglas R Higgs
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

Review 6.  The Skin as an Early Expression of Malignancies in the Neonatal Age: A Review of the Literature and a Case Series.

Authors:  Vito Mondì; Fiammetta Piersigilli; Guglielmo Salvatori; Cinzia Auriti
Journal:  Biomed Res Int       Date:  2015-12-21       Impact factor: 3.411

7.  Clinical course of 63 children with hereditary spherocytosis: a retrospective study.

Authors:  Maria Christina Lopes Araujo Oliveira; Rachel Aparecida Ferreira Fernandes; Carolina Lins Rodrigues; Daniela Aguiar Ribeiro; Maria Fernanda Giovanardi; Marcos Borato Viana
Journal:  Rev Bras Hematol Hemoter       Date:  2012
  7 in total

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