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Congenital absence of kidneys syndrome

Known as: Potter Syndrome, Bilateral Renal Agenesis, Congenital absence of kidneys 
A congenital abnormality characterized by the absence of both kidneys.
National Institutes of Health

Related topics

Related topics

10 relations
Both kidneysCongenital absence of kidneyOligohydramnios sequenceRENAL ADYSPLASIA

Broader (4)

Congenital AbnormalityCongenital absenceKidneyKidney Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
VACTERL association with a rare vertebral anomaly (butterfly vertebra) in a case of monochorionic twin.
The VATER/VACTERL association is typically defined by the presence of at least three of the following congenital malformations… 
1985
1985
Potter's syndrome associated with renal agenesis or dysplasia. Morphological and biochemical study of the lung.
We report on four autopsy cases of Potter's syndrome associated with characteristic Potter's face, pulmonary hypoplasia, and… 
Review
1984
Review
1984
Ultrasound diagnosis and perinatal management of fetal genito-urinary abnormalities.
Approximately 50% of fetal abdominal masses originate in the urinary system and those recognizable ultrasonically include renal… 
1983
1983
Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?
Three sibs, the proband and two monozygotic twins, have a condition including mental retardation, postnatal somatic retardation… 
1981
1981
Birth frequency of bilateral renal agenesis.
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… 
1978
1978
Antenatal diagnosis of Potter syndrome.
: A case is presented of bilateral renal agenesis (Potter syndrome) which was diagnosed before birth. The diagnosis was based on… 
1977
1977
Primary pulmonary hypoplasia: report of a case with polyhydramnios.
We describe a case of extreme primary pulmonary hypoplasia. No other congenital anomalies and none of the conditions known to be… 
1977
1977
Heterogeneity of bilateral renal agenesis.
  • N. Fitch
  • Canadian Medical Association journal
  • 1977
  • Corpus ID: 31446348
Bilateral and unilateral renal agenesis may be expressions of single dominant gene. Chromosome abnormalities may be present and… 
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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