Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Characteristics of very early onset autosomal dominant polycystic kidney disease.

Journal of the American Society of Nephrology : JASN - 1 Jun 1993

Fick G M, Johnson A M, Strain J D, Kimberling W J, Kumar S, Manco-Johnson M L, Duley I T, Gabow P A

Abstract excerpt

Eleven children from eight families with autosomal dominant polycystic kidney disease who were diagnosed in utero (6 children) or in the first year of life (5 children) are reported here. Four children were evaluated for symptoms and three because of a sibling with very early onset disease. In th...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypertension

Share to Kidney

Share to Mutation

Share to Pedigree

Share to Pregnancy

Source

Identifiers

PMID: 8338917
DOI: 10.1681/ASN.V3121863

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-8338917-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characteristics of very early onset autosomal dominant polycystic kidney disease.PMID 8338917Read ↗

Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD).Semantic proximity Read ↗

Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experienceSemantic proximity Read ↗

Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.Semantic proximity Read ↗

Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease.Semantic proximity Read ↗

Phenotypic heterogeneity in pediatric autosomal dominant polycystic kidney disease at first presentation: a single-center, 20-year review.Semantic proximity Read ↗

Diagnostic approach in autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.Semantic proximity Read ↗

Prenatal ultrasound, genotype, and outcome in a large cohort of prenatally affected patients with autosomal-recessive polycystic kidney disease and other hereditary cystic kidney diseases.Semantic proximity Read ↗

Autosomal dominant polycystic kidney disease in the first year of life. Report of a case with no family history.Semantic proximity Read ↗

Neonatal polycystic kidney disease: a novel variant.Semantic proximity Read ↗

The diagnosis and prognosis of autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Clinical practice. Autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.