Jul 1, 1989

Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibships

American Journal of Medical Genetics
A ReussF J Los

Abstract

In 2 consanguineous relationships, a Cape Verdian man fathered six fetuses (5 male) with fetal ventriculomegaly and echodense fetal kidneys as visualized by ultrasonography between 16 and 32 weeks. During prenatal monitoring, an increased alpha fetoprotein level and abnormal acetylcholinesterase were detected at amniocentesis in 5 of 6 affected fetuses. Chromosomes were normal. Five pregnancies resulted in elective termination; one child was still-born prematurely. Hydrocephalus and cystic disease of the (renal) cortico medullary areas were found. One fetus had polydactyly. The differential diagnosis and prenatal diagnosis of this presumably autosomal recessive syndrome are discussed.

  • References11
  • Citations6

References

Mentioned in this Paper

Embryopathies
SDS-PAGE
Antenatal Screening Procedures
Polydactyly
Tomography, Ultrasonic
ACHE
Hydrocephalus
Consanguinous Mating
Cystic Kidney Diseases
Alpha-Fetoproteins

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