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Article

Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndrome.

Prenatal diagnosis - 1 Nov 2006

Viassolo Valeria, Lituania Mario, Marasini Maurizio, Dietz Harry, Benelli Fabrizio, Forzano Francesca, Faravelli Francesca

Abstract excerpt

Loeys-Dietz syndrome is a recently described autosomal dominant disorder with cardinal manifestations in cardiovascular, craniofacial and skeletal systems. Although the disease has some phenotypic overlap with Marfan syndrome, the disease, that is caused by mutations in the transforming growth factor beta-receptor 1 (TGFBR1) or transforming growth factor beta-receptor 2 (TGFBR2) genes, presents many distinctive...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16981219
DOI: 10.1002/pd.1565

Genes

TGFBR1
TGFBR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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