potter syndrome

Potter Syndrome: A case study

  • Anestakis D*, Konstantinidou, Nikolaou A, Moumou G, Karakasi MV, Pavlidis P and Chatzifotiou E

Published on: 31st August, 2017

OCLC Number/Unique Identifier: 7286353788

Potter syndrome (PS) is a term used to describe a typical physical appearance, which is the result of dramatically decreased amniotic fluid volume secondary to renal diseases such as bilateral renal agenesis (BRA). Other causes are abstraction of the urinary tract, autosomal recessive polycystic kidney disease (ARPKD), autosomal dominant polycystic kidney disease (ADPKD) and renal hypoplasia. In 1946, Dr Edith Potter characterized this prenatal renal failure/renal agenesis and the resulting physical characteristics of the fetus/infant that result from oligohydramnios as well as the complete absence of amniotic fluid (anhydramnios). Oligohydramnios and anhydramnios can also be due to the result of leakage of amniotic fluid from rupturing of the amniotic membranes. The case reported below, concerns of stillborn boy with potter syndrome.
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AbstractDOI: 10.29328/journal.jfsr.1001007Read Full Article HTMLRead Full Article PDF

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