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Article

Gonadoblastoma in patients with Ullrich-Turner syndrome.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society - 1 Jan 2000

Zelaya Gabriela, López Marti Jessica M, Marino Roxana, Garcia de Dávila Maria T, Gallego Marta S

Abstract excerpt

Ullrich-Turner syndrome (UTS) is a common chromosomal abnormality caused by partial or complete X chromosome monosomy. One half of the patients have a 45,X karyotype, whereas the remaining patients display other X chromosome anomalies. In 6% to 11% of UTS, a normal or partly deleted Y chromosome has been found. A 10% to 30% risk of developing gonadoblastoma was found in the latter patients. The aim of this study...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25535833
DOI: 10.2350/14-08-1539-OA.1

Genes

SRY

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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Gonadoblastoma in patients with Ullrich-Turner syndrome.PMID 25535833Read ↗

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SRY Gene Increases the Risk of Developing Gonadoblastoma and/or Nontumoral Gonadal Lesions in Turner SyndromeSemantic proximity Read ↗

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Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome.Semantic proximity Read ↗

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PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.Semantic proximity Read ↗

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