Cardiovascular and connective tissue disorder features in FLNA-related PVNH patients: progress towards a refined delineation of this syndrome.
Clarisse BillonSalma AdhamNatalia Hernandez PobleteAnne LegrandMichael FrankLaurent ChicheStephane ZuilyKarelle BenistanLaurent SavaleKhaoula Zaafrane-KhachnaouiAnne-Claire BrehinLaurence BalTiffany BusaMélanie FradinChloé QuelinBertrand ChesneauDenis WahlPatricia FergelotCyril GoizetTristan MiraultXavier JeunemaitreJuliette Albuissonnull nullPublished in: Orphanet journal of rare diseases (2021)
In FLNA LoF patients, the absence of seizures should not be overlooked. When considering a diagnosis of PVNH1, the assessment for CV and CTD anomalies is of major interest as they represent interlinked features. We recommend systematic study of FLNA within CTD genes panels, regardless of the presence of neurological symptoms.