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M HERVE MBIANDJI

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Auteur de référence en rhumatologie
22 articles scientifiques publiés — un praticien à la pointe de la recherche

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Top publications · les plus citées

COL4A1 and COL4A2 Gene Duplication or Triplication as a Genetic Cause of Cerebral Small Vessel Disease in Adults

Stroke · 2026

📚 2 citations

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BACKGROUND: Cerebral small vessel disease (CSVD) is a major cause of stroke and vascular cognitive impairment, yet its mechanisms remain incompletely understood. While heterozygous point mutations in COL4A1 and COL4A2 are established monogenic cause of CSVD, the contribution of copy number gains involving these 2 genes has only recently been recognized. We aimed to define the clinical and radiological spectrum of COL4A1/2 duplications and triplications in adults. METHODS: We report 7 adult probands carrying duplications or triplications of COL4A1 and COL4A2 , in whom no pathogenic variants were identified in other known CSVD genes. Targeted high-throughput sequencing, quantitative multiplex polymerase chain reaction of short fluorescent fragments, and SNP arrays were used to confirm and characterize genomic rearrangements spanning the 13q33q34 region. RESULTS: Genomic rearrangements ranged from 328 kb to 11.8 Mb, involving complete or partial duplication/triplication of COL4A1/2 . Patients presented heterogeneous cerebrovascular manifestations, including ischemic and hemorrhagic events, motor impairment, and cognitive decline. Brain magnetic resonance imaging consistently showed extensive white matter hyperintensities, lacunes (particularly in the pons), microbleeds, and, in some cases, saccular aneurysms or arterial dolichoectasia. Only 2 probands had a positive family history of CSVD. CONCLUSIONS: This large series confirms the pathogenicity of COL4A1/2 duplications and triplications in adult-onset CSVD. Phenotypic variability likely reflects differences in duplication/triplication size, gene content, and modifying factors. Our findings highlight a distinct cerebral-only phenotype linked to gene dosage–related overexpression and underscore the importance of screening for copy number variations in patients with otherwise unexplained cerebral microangiopathy, even in the absence of a family history.

Navigating the waters of LUTS from childhood to puberty - NOPIA meeting (ICI-RS 2024)

Journal of pediatric urology · 2025

📚 2 citations🔓 Open Access

Trends in surgical treatment of female stress urinary incontinence in France over the past decade (2015-2024)

The French journal of urology · 2026

📚 1 citations🔓 Open Access

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M HERVE MBIANDJI

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Publications scientifiques (22) — classées par pathologie

Revue générale9

Génétique4

Transversal4

Essai clinique2

Gériatrie1

Pédiatrie1

Revue / méta-analyse1

Rhumatisme psoriasique1

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