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Article

Lower extremity amputation in a preterm infant due to MTHFR homozygosity.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2014

Bekmez S, Beken S, Dinc T, Dursun A, Zenciroglu A, Dilli D, Okumus N

Abstract excerpt

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Topics

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Share to Gestational Age
Share to Homozygote
Share to Infant, Premature
Share to Lower Extremity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Pregnancy

Share to Thrombosis

Source

Identifiers

PMID: 25059027

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Lower extremity amputation in a preterm infant due to MTHFR homozygosity.PMID 25059027Read ↗

Dual mutation (MTHFR A1298C with PAI (4G) mutation) manifesting with bilateral lower limb gangrene in a neonate.Semantic proximity Read ↗

Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defects.Semantic proximity Read ↗

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