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Article

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

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin - 1 Apr 2004

Riebel T, Köchling J, Scheer I, Oellinger J, Reis A

Abstract excerpt

PURPOSE: The imaging documents, obtained in connection with a primarily molecular genetic study on Currarino syndrome, should be evaluated with special respect to the constancy resp. the variability of findings in patients with proven HLBX9 mutations. METHODS: In five female non-related index patients with clinico-radiologically diagnosed Currarino syndrome and further 53 members of their families, changes of the...

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Identifiers

PMID: 15088182
DOI: 10.1055/s-2004-812948

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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