Medizinische Universität Graz - Research portal

Go directly to the nagivation.
Go directly to the content.

Navigation/Search

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Borroto, MC; Patel, H; Srivastava, S; Swanson, LC; Keren, B; Whalen, S; Mignot, C; Wang, X; Chen, Q; Rosenfeld, JA; McLean, S; Littlejohn, RO; Emrick, L; Burrage, LC; Attali, R; Lesca, G; Acquaviva-Bourdain, C; Sarret, C; Seaver, LH; Platzer, K; Bartolomaeus, T; Wünsch, C; Fischer, S; Rodriguez, Barreto, AM; Granadillo, JL; Schreiner, E; Brunet, T; Schatz, UA; Thiffault, I; Mullegama, SV; Michaud, JL; Hamdan, FF; Rossignol, E; Campeau, PM, , Undiagnosed, Diseases, Network.
Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder.
Pediatr Neurol. 2024; 160: 45-53. Doi: 10.1016/j.pediatrneurol.2024.07.010
Web of Science PubMed FullText FullText_MUG

Co-authors Med Uni Graz: Schreiner Elisabeth
Altmetrics:
Dimensions Citations:
Plum Analytics:
Scite (citation analytics):
Abstract:: BACKGROUND: GTPases of the Rab family are important orchestrators of membrane trafficking, and their dysregulation has been linked to a variety of neuropathologies. In 2017, we established a causal link between RAB11A variants and developmental and epileptic encephalopathy. In this study, we expand the phenotype of RAB11A-associated neurodevelopmental disorder and explore genotype-phenotype correlations. METHODS: We assessed 16 patients with pathogenic or likely pathogenic RAB11A variants, generally de novo, heterozygous missense variants. One individual had a homozygous nonsense variant, although concomitant with a pathogenic LAMA2 variant, which made their respective contributions to the phenotype difficult to discriminate. RESULTS: We reinforce the finding that certain RAB11A missense variants lead to intellectual disability and developmental delays. Other clinical features might include gait disturbances, hypotonia, magnetic resonance imaging abnormalities, visual anomalies, dysmorphisms, early adrenarche, and obesity. Epilepsy seems to be less common and linked to variants outside the binding sites. Individuals with variants in the binding sites seem to have a more multisystemic, nonepileptic phenotype. CONCLUSIONS: Similar to other Rab-related disorders, RAB11A-associated neurodevelopmental disorder can also impact gait, tonus, brain anatomy and physiology, vision, adrenarche, and body weight and structure. Epilepsy seems to affect the minority of patients with variants outside the binding sites.
Find related publications in this database (Keywords): RAB11; GTPase; Neurodevelopmental disorder; Epileptic encephalopathy