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Article

Mesenteric venous thrombosis in a child with type 2 protein S deficiency.

Journal of pediatric hematology/oncology - 1 Mar 2011

Hayakawa Takahiro, Morimoto Akira, Nozaki Yasuyuki, Kashii Yoshifumi, Aihara Toshinori, Maeda Kosaku, Momoi Mariko Y

Abstract excerpt

A 5-year-old girl presented with abdominal pain and bloody stools 2 weeks after suffering from influenza A infection. Enhanced computed tomographic scan showed widespread splanchnic venous thrombosis and small intestine necrosis. She recovered after the necrotic bowel was resected. The patient continues to receive anticoagulant therapy. Thrombophilia screening after the complete resolution consistently showed...

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Source

Identifiers

PMID: 21285903
DOI: 10.1097/MPH.0b013e3181fce4d4

Genes

PROS1

Provenance

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.

Related research

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Research trail→

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Mesenteric venous thrombosis in a child with type 2 protein S deficiency.PMID 21285903Read ↗

[Hereditary protein S deficiency in a patient with prominent mesenteric venous thrombosis: A case report].Semantic proximity Read ↗

Recurrent pulmonary embolism associated with deep venous thrombosis diagnosed as protein s deficiency owing to a novel mutation in PROS1: A case report.Semantic proximity Read ↗

Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study.Semantic proximity Read ↗

A rare splicing mutation in the PROS1 gene of a Korean patient with type I hereditary protein S deficiency.Semantic proximity Read ↗

Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia.Semantic proximity Read ↗

A new hereditary PROS1 mutation caused isolated cortical venous thrombosis: a case report and literature reviewSemantic proximity Read ↗

Genotype and laboratory and clinical phenotypes of protein s deficiency.Semantic proximity Read ↗

A new hereditary PROS1 gene mutation caused isolated cortical venous thrombosis.Semantic proximity Read ↗

[PROSI Mutation With Clinical Heterogeneity in Protein S Deficiency:Report of One Case].Semantic proximity Read ↗

One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.Semantic proximity Read ↗

Protein S Erlangen: a novel PROS1 gene mutation associated with quantitative protein S deficiency.Semantic proximity Read ↗

A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohort.Semantic proximity Read ↗

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