Improving Hereditary Hemorrhagic Telangiectasia Molecular Diagnosis: A Referral Center Experience.
Cinthia AguileraAriadna Padró-MiquelAnna Esteve-GarciaPau CerdàRaquel Torres-IglesiasNúria LlechaAntoni Riera-MestrePublished in: Genes (2023)
RNA analysis should be performed to assess and/or confirm the impact of variants on splicing. The molecular diagnosis of HHT patients is crucial to allow family screening and accurate genetic counseling. A multidisciplinary approach including clinicians and geneticists is crucial when dealing with patients with rare diseases.