Article

Pediatric Cerebral Infarction Unraveled: A Case of MTHFR Mutation and Hyperhomocysteinemia-Case Report

2024-12-10

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold> Cerebral infarction in children without underlying diseases is rare, and its causes are complex. <bold>Case presentation</bold> We present a case of a 14-year-old boy who experienced left limb weakness and slurred speech for 5 days. MRI revealed cerebral infarction in the bilateral occipital lobes and right centrum semiovale, with high homocysteine levels. He was...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 4f546cb3-5667-5a2f-b785-6fe9fa77bdf5
DOI: 10.21203/rs.3.rs-5212213/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Pediatric Cerebral Infarction Unraveled: A Case of MTHFR Mutation and Hyperhomocysteinemia-Case ReportDOI 10.21203/rs.3.rs-5212213/v1Read

Watershed infarction during the first favism crisis in a Syrian child; A rare case reportSemantic proximity Read

A Tall and Thin Boy with a Bad Headache: A Case Report of HomocystinuriaSemantic proximity Read

Early-Onset Moyamoya Disease Presentingwith Recurrent Seizures and Dysphagia in a3.5-Year-Old Child: A Case ReportSemantic proximity Read

Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency.Semantic proximity Read

Etiology of stroke in children.Semantic proximity Read

The role of genetic risk factors in arterial ischemic stroke in pediatric and adult patients: a critical review.Semantic proximity Read

Bilateral Cerebrovascular Accident in Pediatric Sickle Cell Anemia: A Cascade of Complications – A Case ReportSemantic proximity Read

Monogenetic Stroke Syndromes in Children and Young Adults.Semantic proximity Read

Focal cerebral arteriopathy in adults: A single centre experienceSemantic proximity Read

Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.Semantic proximity Read

The TT genotype of methylenetetrahydrofolate reductase 677C>T polymorphism increases the susceptibility to pediatric ischemic stroke: meta-analysis of the 822 cases and 1,552 controls.Semantic proximity Read

Guidelines for diagnosis and management of the cobalamin‐related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiencySemantic proximity Read