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.
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Authors | M C Dauge-Geffroy |
Journal | Annales de pathologie
(Ann Pathol)
Vol. 17
Issue 4
Pg. 295-9
(Sep 1997)
ISSN: 0242-6498 [Print] France |
Vernacular Title | Que rechercher dans un contexte d'oligoamnios? |
PMID | 9409891
(Publication Type: English Abstract, Journal Article, Review)
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Topics |
- Female
- Fetus
(pathology)
- Humans
- Maternal-Fetal Exchange
- Oligohydramnios
(pathology)
- Placenta
(pathology)
- Pregnancy
- Research
- Syndrome
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