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Article

Cerebral ultrasound abnormalities in offsprings of women with C677T homozygous mutation in the MTHFR gene: a prospective study.

World journal of pediatrics : WJP - 1 May 2015

Pogliani Laura, Cerini Chiara, Penagini Francesca, Duca Piergiorgio, Mameli Chiara, Zuccotti Gian Vincenzo

Abstract excerpt

BACKGROUND: Perinatal stroke is a common cause of neurologic disability. Being clinically under-recognized, its true incidence is not known. Maternal thrombophilia is likely to be a predisposing factor. To date, a general consensus for evaluation of babies born to mothers with genetic thrombotic predisposition is missing. This study was undertaken to assess the frequency of cerebral abnormalities in the offspring...

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Share to Cerebrovascular Disorders
Share to Homozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Incidence

Share to Infant, Newborn

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation, Missense

Share to Risk Factors

Share to Ultrasonography

Source

Identifiers

PMID: 24974211
DOI: 10.1007/s12519-014-0490-0

Genes

MTHFR

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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