Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Neonatal bilateral cerebral high flow fistulae leading to detection of a HHT-family carrier.

Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences - 1 Aug 2021

Alvarez Hortensia, Niazi Muhammad H, Loewenstein Joshua, Quinsey Carolyn S

Abstract excerpt

Cerebral and spinal cord high-flow arteriovenous fistulae (HFAVF) are part of the spectrum of lesions found in Hereditary Hemorrhagic Telangiectasia (HHT). HFAVF consist of communications between large arteries and veins without interposed nidi or capillary transitions. The association between HHT and cerebral or spinal HFAVF in children has been reported and suggested as a potential marker for HHT. We present a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Mutation

Share to Spinal Cord

Share to Telangiectasia, Hereditary Hemorrhagic

Source

Open in PubMed Open full text

Identifiers

PMID: 33353465
DOI: 10.1177/1591019920981308
PMCID: PMC8580537

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

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neonatal bilateral cerebral high flow fistulae leading to detection of a HHT-family carrier.PMID 33353465Read ↗

Clinical and genetic findings in children with central nervous system arteriovenous fistulas.Semantic proximity Read ↗

A spectrum of intracranial vascular high-flow arteriovenous shunts in RASA1 mutations.Semantic proximity Read ↗

Family Phenotypic Profile in Hereditary Hemorrhagic Telangiectasia: Genotype-Phenotype Correlation in the Pediatric PopulationSemantic proximity Read ↗

[Cerebral sinovenous thrombosis in a newborn with mutation of MTHFR C677T treated with enoxaparin].Semantic proximity Read ↗

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

[Hereditary hemorrhagic telangiectasia: a report of two cases].Semantic proximity Read ↗

A newborn with hereditary haemorrhagic telangiectasia and an unusually severe phenotype.Semantic proximity Read ↗

Neurovascular phenotypes in hereditary haemorrhagic telangiectasia patients according to age. Review of 50 consecutive patients aged 1 day-60 years.Semantic proximity Read ↗

Manifestations of thrombospondin type-1 domain-containing protein 1 gene mutation in an extremely premature infant with nonimmune hydrops fetalis.Semantic proximity Read ↗

Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.Semantic proximity Read ↗

Heterozygous methylenetetrahydrofolate reductase 677C-T gene mutation with mild hyperhomocysteinemia associated with intrauterine iliofemoral artery thrombosis.Semantic proximity Read ↗

Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.