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Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays.

Prenatal diagnosis - 1 Apr 2014

Kasatkar Priyanka, Shetty Shrimati, Ghosh Kanjaksha

Abstract excerpt

OBJECTIVE: This study aimed to offer genetic diagnosis to affected type 3 severe von Willebrand disease families. METHOD: Thirteen families were referred for prenatal diagnosis during the first and second trimesters of pregnancy. Prenatal diagnosis was offered by chorionic villus sampling between 11 and 12 weeks and by cordocentesis between 18 and 19.5 weeks of gestation. Phenotypic analysis included FVIII:C and...

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PMID: 24390653
DOI: 10.1002/pd.4315

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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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