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Article

Prenatal testing in Huntington disease: after the test, choices recommence.

European journal of human genetics : EJHG - 1 Nov 2016

Bouchghoul Hanane, Clément Stéphane-Françoise, Vauthier Danièle, Cazeneuve Cécile, Noel Sandrine, Dommergues Marc, Héron Delphine, Nizard Jacky, Gargiulo Marcela, Durr Alexandra

Abstract excerpt

The objective of this study was (1) to determine the impact of prenatal diagnosis (PND) for Huntington disease (HD) on subsequent reproductive choices and family structure; and (2) to assess whether children born after PND were informed of their genetic status. Out of 354 presymptomatic carriers of HD gene mutation, aged 18-45 years, 61 couples requested 101 PNDs. Fifty-four women, 29 female carriers and 25...

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Identifiers

PMID: 27302844
DOI: 10.1038/ejhg.2016.59
PMCID: PMC5110058

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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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