Literature DB >> 17377610

Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis.

S Yetgin1, S Aytac, F Gurakan, M Yurdakok.   

Abstract

Nonimmune hydrops fetalis may occur as a result of different etiological conditions and in about one-third of cases no cause could be identified. Here, we report two cases of nonimmune hydrops fetalis associated with hereditary spherocytosis and hemophagocytic hystiocytosis. We think that babies with hydrops fetalis born of consanguineous parents should be examined for hereditary diseases, and that these rare causes should be taken into account in problematic cases.

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Year:  2007        PMID: 17377610     DOI: 10.1038/sj.jp.7211657

Source DB:  PubMed          Journal:  J Perinatol        ISSN: 0743-8346            Impact factor:   2.521


  3 in total

1.  Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis.

Authors:  Dawn M Hannah; Terry B Tressler; Claudia D Taboada
Journal:  Case Rep Womens Health       Date:  2017-10-02

2.  Comparative Proteomic Assessment of Normal vs. Polyhydramnios Amniotic Fluid Based on Computational Analysis.

Authors:  Rūta Navakauskienė; Sandra Baronaitė; Dalius Matuzevičius; Natalija Krasovskaja; Gražina Treigytė; Audronė Arlauskienė; Dalius Navakauskas
Journal:  Biomedicines       Date:  2022-07-28

3.  Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis: A case report.

Authors:  Yimin Zhang; Shuming Shao; Jie Liu; Chaomei Zeng; Ye Han; Xiaorui Zhang
Journal:  Medicine (Baltimore)       Date:  2021-03-26       Impact factor: 1.817

  3 in total

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