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Oligohydramnios sequence

Known as: Potter Syndrome, Potter's Sequence, Potter sequence 
A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid… 
National Institutes of Health

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Congenital absence of kidneys syndromeHereditary Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
1995
Review
1995
Urinary tract anomalies detected by prenatal ultrasound examination at Mayo Clinic Rochester.
OBJECTIVE To determine the frequency of fetal urinary tract anomalies and to characterize the types of such abnormalities… 
Review
1993
Review
1993
Fetal Hemivertebrae: Associated Anomalies, Significance, and Outcome
Objective: To study fetuses who had the sonographic diagnosis of hemivertebrae made in utero (excluding open neural tube defects… 
1990
1990
Erythropoietin levels and erythropoiesis at birth in infants with Potter syndrome.
1986
1986
In vivo lactate production and utilization by Jensen sarcoma and Morris hepatoma 7288CTC.
These experiments were designed to determine the characteristics of lactic acid utilization and production in vivo in Jensen… 
1983
1983
Indomethacin and the fetal renal nonfunction syndrome.
1982
1982
Multiple Acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers
The post mortem and microscopic findings of two newborn male sibling of Turkish origin suffering from multiple acyl-CoA… 
1980
1980
Congenital cystic adenomatoid malformation in bilateral renal agenesis. Its mitigation of Potter's syndrome.
Potter's syndrome develops secondary to a deficiency of amniotic fluid, such as occurs in renal agenesis. Congenital cystic… 
1977
1977
Prenatal Diagnosis of Bilateral Renal Agenesis
Bilateral renal agenesis (BRA), or Potter's syndrome, is a rare genetic disorder in which agenesis of the kidneys is associated… 
1974
1974
Lung perforation during chest tube placement in the stiff lung syndrome.
1972
1972
An unusual case of sirenomelia.
A report is presented of a case of sirenomelia (symmelos). The affected infant was a partner in a monozygous monoamniotic twin… 
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