Clinical Genetics · 1998 · 10 citations · 16 references
MedicineGeneticsNephrologyPediatric NephrologyRenal PathologyRenal PathophysiologyCongenital Renal AnomaliesHereditary Kidney DiseasesHereditary Renal DiseasesRenal Cystic DiseasesRenal DiseaseRenal ImagingCongenital Kidney DiseaseCongenital Kidney DisordersFetal Kidney ImagingHereditary Cystic Kidney DiseasePaternal TransmissionPrenatal Renal AnomaliesPrenatal Renal UltrasoundRenal Corticomedullary Differentiation
We present a family with adult onset autosomal dominant polycystic kidney disease (ADPKD) in two generations, linked to the PKD1 locus and with paternal transmission to the fetus. The fetus carried the PKD1 haplotype and was, therefore a gene carrier. Progressive hyperechogenic renal enlargement, but no cysts, was documented by serial fetal ultrasounds at 21, 23 and 34 weeks of gestation. Surprisingly, the newborn renal scan showed normal sized kidneys with apparently normal corticomedullary differentiation. However, at 11 months of age, the evolution of cysts in one kidney, and then in the other kidney at 20 months, was documented by ultrasound in the absence of clinical symptoms or signs. The observed normalisation of fetal renal ultrasound appearances at birth has not previously been described in fetuses presenting with PKD1.
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Reserpine and Gastric Secretion in Man
A. R. Krogsgaard · Acta Medica Scandinavica · 1957 · 315 citations
Medicine, Pharmacology, Physiology +12
Sonographic assessment of renal length in normal children
DM Rosenbaum, Elena Korngold, Teele Rl · American Journal of Roentgenology · 1984 · 314 citations
Medicine, Nephrology, Pediatrics +14