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Article

Malignant degeneration of presacral teratoma in the Currarino anomaly.

American journal of medical genetics. Part A - 30 Jul 2004

Urioste Miguel, Garcia-Andrade M del Carmen, Valle Laura, Robledo Mercedes, González-Palacios Fernando, Méndez Ramiro, Ferreirós Joaquin, Nuño Javier, Benítez Javier

Abstract excerpt

The autosomal dominant Currarino anomaly (CA) comprises a presacral mass, partial sacral agenesis, and anorectal defects. Chronic constipation in childhood related to anorectal defects is the most common presenting symptom and hemisacrum the most frequent malformation. The presacral mass may be a...

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Source

Identifiers

PMID: 15216552
DOI: 10.1002/ajmg.a.30028

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15216552-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

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Research trail→

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Malignant degeneration of presacral teratoma in the Currarino anomaly.PMID 15216552Read ↗

Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodynia.Semantic proximity Read ↗

[Currarino syndrome: variability of imaging findings in 22 molecular-genetically identified (HLXB9 mutation) patients from five families].Semantic proximity Read ↗

Autosomal dominant sacral agenesis: Currarino syndromeSemantic proximity Read ↗

[Currarino syndrome--a case report].Semantic proximity Read ↗

Currarino triad with dual pathology in the presacral mass: report of a case.Semantic proximity Read ↗

Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.Semantic proximity Read ↗

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.Semantic proximity Read ↗

Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.Semantic proximity Read ↗

The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndrome.Semantic proximity Read ↗

Currarino syndrome: variable imaging features in three siblings with HLXB9 gene mutation.Semantic proximity Read ↗

Currarino syndrome at Rikshospitalet 1961-2012.Semantic proximity Read ↗

Currarino syndrome: proposal of a diagnostic and therapeutic protocol.Semantic proximity Read ↗

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