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[How to research oligohydramnios?].

Abstract
When an oligohydramnios has been clinically detected, the fetoplacental study has to find the cause of this syndrome: malformations, infectious or environmental anomalies, and to study the consequences of this syndrome in the fetus. A careful and complete study allows us to indicate some genic syndromes such as polycystic kidney disease, Meckel syndrome, familial renal tubular dysgenesis, Vacterl-Hydrocephaly sequence, or Fraser syndrome inducing the genetic counseling and a familial study. The other pathologies, such as maternal diseases, infections or sporadic malformations must be followed by cautious maternal care for subsequent pregnancies.
AuthorsM C Dauge-Geffroy
JournalAnnales de pathologie (Ann Pathol) Vol. 17 Issue 4 Pg. 295-9 (Sep 1997) ISSN: 0242-6498 [Print] France
Vernacular TitleQue rechercher dans un contexte d'oligoamnios?
PMID9409891 (Publication Type: English Abstract, Journal Article, Review)
Topics
  • Female
  • Fetus (pathology)
  • Humans
  • Maternal-Fetal Exchange
  • Oligohydramnios (pathology)
  • Placenta (pathology)
  • Pregnancy
  • Research
  • Syndrome

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