Literature DB >> 11816486

Hydrops fetalis.

R Bukowski1, G R Saade.   

Abstract

Although most NIH fetuses have poor prognosis, it is imperative to attempt to identify the underlying cause to present parents with the best estimate for prognosis and future outcomes. Identification of a disorder with a good prognosis may prevent unnecessary termination of pregnancy and give a chance for therapy. Identification of a disorder with poor prognosis may still provide information that may be unavailable after delivery regarding this and future pregnancies.

Mesh：

Year:  2000        PMID： 11816486     DOI： 10.1016/s0095-5108(05)70061-0

Source DB:  PubMed          Journal:  Clin Perinatol        ISSN： 0095-5108            Impact factor:   3.430


  3 in total

1.  The many faces of hydrops.

Authors:  S Christopher Derderian; Cerine Jeanty; Shannon R Fleck; Lily S Cheng; Shabnam Peyvandi; Anita J Moon-Grady; Jody Farrell; Shinjiro Hirose; Juan Gonzalez; Roberta L Keller; Tippi C MacKenzie
Journal:  J Pediatr Surg       Date:  2014-10-29       Impact factor: 2.545

2.  hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia.

Authors:  Duncan I Mackie; Fuad Al Mutairi; Reema B Davis; Daniel O Kechele; Natalie R Nielsen; Joshua C Snyder; Marc G Caron; Harvey J Kliman; Jonathan S Berg; John Simms; David R Poyner; Kathleen M Caron
Journal:  J Exp Med       Date:  2018-08-16       Impact factor: 17.579

Review 3.  Congenital pulmonary lymphangiectasia.

Authors:  Carlo Bellini; Francesco Boccardo; Corradino Campisi; Eugenio Bonioli
Journal:  Orphanet J Rare Dis       Date:  2006-10-30       Impact factor: 4.123
  3 in total

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