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Article

A girl with bilateral ovarian tumours: Frasier syndrome.

European journal of pediatrics - 1 Feb 2002

Shimoyama Hironobu, Nakajima Mitsuru, Naka Hiroyuki, Park Yong-Dong, Hori Kensuke, Morikawa Hajime, Yoshioka Akira

Abstract excerpt

UNLABELLED: Frasier syndrome (FS) is characterised by male pseudohermaphroditism, slowly progressing nephropathy and frequent development of gonadoblastoma. The Wilms' tumour suppressor gene (WT1 gene) plays an important role in the development of the urogenital system and the gonads. A splice mu...

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Source

Identifiers

PMID: 11954756
DOI: 10.1007/s00431-001-0867-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11954756-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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A girl with bilateral ovarian tumours: Frasier syndrome.PMID 11954756Read ↗

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Frasier syndrome: four new cases with unusual presentations.Semantic proximity Read ↗

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

Bilateral Gonadoblastoma in a 6-Year-old Girl With Frasier Syndrome: Need for Early Preventive Gonadectomy.Semantic proximity Read ↗

Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis.Semantic proximity Read ↗

Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes).Semantic proximity Read ↗

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