Smith-Kingsmore syndrome associated neurovascular complications and stroke: report of two cases

European Journal of Medical Genetics · Published 2026-07-16 · DOI 10.1016/j.ejmg.2026.105094

Free full text

Authors (5)

Eoin P. Donnellan, Erin L. Langton, Ailbhe Moran, Elaine Reade, Nicholas M. Allen

Abstract

PubPorta does not have an abstract for this article yet.

Read the article at the publisher →

Publication details

Year

2026

Citation

Donnellan, E., Langton, E., Moran, A., et al. (2026). Smith-Kingsmore syndrome associated neurovascular complications and stroke: report of two cases. European Journal of Medical Genetics. https://doi.org/10.1016/j.ejmg.2026.105094

Related articles

• Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses · Genome Medicine · 2022 · Cites or is cited by this article
• Phenotypic discordance in monozygotic twins with a CDH2 variant · European Journal of Medical Genetics · 2026 · Same journal
• Pathogenic variant in GATA4 associated with atrioventricular septal defect and congenital diaphragmatic hernia: A case report · European Journal of Medical Genetics · 2025 · Same journal
• A fetal case of Stüve-Wiedemann syndrome due to a novel homozygous truncating variant in IL6ST · European Journal of Medical Genetics · 2025 · Same journal
• Tachycardiomyopathy-like presentation in neonatal MCAD deficiency: A novel cardiac phenotype · European Journal of Medical Genetics · 2026 · Same journal
• Rare features in Feingold syndrome type 1 · European Journal of Medical Genetics · 2025 · Same journal
• Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literature · European Journal of Medical Genetics · 2026 · Same journal
• Chromosome heteromorphisms: Critical literature review finds No convincing evidence of harm · European Journal of Medical Genetics · 2025 · Same journal
• COL12A1-related myopathic Ehlers–Danlos syndrome with Chiari I malformation: A clinical report · European Journal of Medical Genetics · 2025 · Same journal
• Cost-comparison of resequencing versus archival data methods for periodic reanalysis of genomic data in rare diseases diagnosis: A UK pilot analysis · European Journal of Medical Genetics · 2025 · Same journal