Literature DB >> 7985044

Nonimmune hydrops fetalis.

M E Norton1.   

Abstract

In summary, NIHF is a heterogenous disorder resulting from a vast number of underlying pathologies. A thorough evaluation should be performed in all cases to attempt to establish the etiology. This requires a systematic approach that should logically proceed from least to most invasive testing. Despite increasing availability of treatment for some causes of NIHF, the prognosis for this condition in general remains poor. In cases of fetal or neonatal demise, autopsy should be encouraged to aid in confirming or making a diagnosis. It is especially important to rule out potentially treatable conditions, as well as genetic disorders with a risk of recurrence in future pregnancies.

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Mesh:

Year:  1994        PMID: 7985044

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


  3 in total

1.  Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.

Authors:  Gwendolyn de Bruyn; Alexandra Casaer; Katrien Devolder; Geert Van Acker; Hilde Logghe; Koen Devriendt; Luc Cornette
Journal:  Eur J Pediatr       Date:  2011-09-15       Impact factor: 3.183

2.  Retrospective study of prenatal diagnosed pulmonary sequestration.

Authors:  Haichun Zhang; Junzhang Tian; Zhongping Chen; Xiaoyan Ma; Gang Yu; Jiangyu Zhang; Guihua Jiang; Limin Wang
Journal:  Pediatr Surg Int       Date:  2013-11-21       Impact factor: 1.827

Review 3.  Lysosomal storage disorder in non-immunological hydrops fetalis (NIHF): more common than assumed? Report of four cases with transient NIHF and a review of the literature.

Authors:  Catharina Whybra; Eugen Mengel; Alexandra Russo; Franz Bahlmann; Christoph Kampmann; Michael Beck; Elke Eich; Eva Mildenberger
Journal:  Orphanet J Rare Dis       Date:  2012-11-08       Impact factor: 4.123

  3 in total

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