Literature DB >> 6391171

Investigation of nonimmune hydrops fetalis.

W Holzgreve, C J Curry, M S Golbus, P W Callen, R A Filly, J C Smith.   

Abstract

Fifty pregnancies complicated by fetal ascites and generalized edema are reviewed and their prenatal findings, obstetric management, and fetal outcome are discussed. From the myriad of maternal, fetal, and placental problems which are known to cause nonimmune hydrops fetalis, many different causes of the disorder could be identified in 84% of all patients studied by extensive prenatal and postnatal workup. Therefore, in only 16% of the cases was the nonimmune hydrops fetalis labeled "idiopathic." The most common demonstrable causes of the disorder in this series were cardiac anomalies, followed by chromosomal disorders, congenital malformations, alpha-thalassemia, and the twin-twin transfusion syndrome. A systematic approach to the prenatal diagnostic workup of nonimmune hydrops fetalis is outlined, starting with the least invasive techniques (ultrasound, echocardiography, complete blood count, Kleihauer-Betke analysis, TORCH testing, and so forth) followed by more invasive techniques (amniocentesis and fetoscopy). Although the detection and prognostic evaluation of nonimmune hydrops fetalis are greatly improved by applying these techniques, the overall prognosis for most fetuses with nonimmune hydrops fetalis is still very poor, and only a few conditions causing the disorder, such as prenatally detected cardiac arrhythmias or selected cases of urinary tract obstruction, are amenable to treatment in utero.

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Year:  1984        PMID: 6391171     DOI: 10.1016/0002-9378(84)90453-8

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  8 in total

1.  Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy.

Authors:  P Steenhout; C Elmer; A Clercx; D Blum; D Gnat; S van Erum; F Vertongen; E Vamos
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli.

Authors:  G Schwanitz; K Zerres; U Gembruch; R Bald; M Hansmann
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

3.  Hydrops fetalis caused by a blood group antibody usually undetected in routine screening.

Authors:  J Smoleniec; N Anderson; G Poole
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1994-11       Impact factor: 5.747

4.  Diagnosis and management of non-immune hydrops in the newborn.

Authors:  T Stephenson; J Zuccollo; M Mohajer
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1994-03       Impact factor: 5.747

5.  Increased level of second trimester maternal serum chorionic gonadotropin in pregnancy with a fetus affected by homozygous alpha-thalassemia 1.

Authors:  L H Tseng; H L Hwa; S M Chuang; T Y Lee; T M Ko
Journal:  Arch Gynecol Obstet       Date:  1994       Impact factor: 2.344

Review 6.  Alpha-thalassaemia.

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

Review 7.  Cardiac ultrasonography in structural abnormalities and arrhythmias. Recognition and treatment.

Authors:  M M Brook; N H Silverman; M Villegas
Journal:  West J Med       Date:  1993-09

8.  The changing pattern of fetal hydrops.

Authors:  D C Wilson; H L Halliday; G McClure; M M Reid
Journal:  Ulster Med J       Date:  1990-10
  8 in total

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