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Article

Case report: Teenage girl with proteinuria and amenorrhea.

Current opinion in pediatrics - 1 Apr 2001

Hausladen J, Granahan E, Bockenhauer D

Abstract excerpt

Recent research has advanced the understanding of many diseases to a molecular level. Described here is the case of a teenage girl with proteinuria and primary amenorrhea. We present the current knowledge of her underlying disorder, Frasier syndrome, and its genetic basis, which are specific mutations in the Wilms tumor gene. The findings in Frasier syndrome research are contrasted with those of a related...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glomerulosclerosis, Focal Segmental

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Source

Identifiers

PMID: 11317057
DOI: 10.1097/00008480-200104000-00011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case report: Teenage girl with proteinuria and amenorrhea.PMID 11317057Read ↗

Expanding the clinical spectrum of Frasier syndrome.Semantic proximity Read ↗

A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review.Semantic proximity Read ↗

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?Semantic proximity Read ↗

[WT1 mutation as a cause of progressive nephropathy in Frasier syndrome--case report].Semantic proximity Read ↗

Frasier syndrome with childhood-onset renal failure.Semantic proximity Read ↗

End-stage renal disease and primary hypogonadism associated with a 46,XX karyotype.Semantic proximity Read ↗

Frasier syndrome: a rare cause of delayed puberty.Semantic proximity Read ↗

Absent pubertal development in a child with chronic renal failure: the case of Frasier syndrome.Semantic proximity Read ↗

Lack of puberty despite elevated estradiol in a 46,XY phenotypic female with Frasier syndrome.Semantic proximity Read ↗

WT1 gene mutations in three girls with nephrotic syndrome.Semantic proximity Read ↗

[Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology].Semantic proximity Read ↗

A girl with bilateral ovarian tumours: Frasier syndrome.Semantic proximity Read ↗

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