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Article

A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy.

Prenatal diagnosis - 1 Nov 2008

Ma Gwo-Chin, Liu Chin-San, Chang Shun-Ping, Yeh Kun-Tu, Ke Yu-Yuan, Chen Tze-Ho, Wang Boris Bao-Tyan, Kuo Shou-Jen, Shih Jin-Chung, Chen Ming

Abstract excerpt

OBJECTIVES: To assess the possible correlations between the reported candidate genes (VEGFR3, FOXC2, ITGA9 and ITGB1) and the clinical response in fetuses with severe congenital chylothorax (CC) treated by prenatal OK-432 pleurodesis. METHODS: We studied 12 unrelated fetuses with severe CC, recei...

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Source

Identifiers

PMID: 18973153
DOI: 10.1002/pd.2130

Genes

ITGA9
FOXC2
ITGB1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18973153-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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