Come contattare il centro
Centro HCP
Gli obiettivi del centro sono:
Fornire al paziente e alla sua famiglia un'assistenza medica (oftalmologica e genetica in particolare), ortottica (riabilitazione, ipovisione), psicologica e sociale coerente e completa.
Garantire un collegamento con i medici curanti e i corrispondenti, le reti mediche e psicosociali di gestione dell'ipovisione e le associazioni dei pazienti.
Sviluppare e partecipare a programmi di ricerca dedicati alla genetica oftalmologica a livello locale, nazionale e internazionale.
Contatti
CARGO, Hôpitaux Universitaires de Strasbourg, France
Team
Pr Hélène Dollfus
Francia
Dr Monika Grudzinska Pechhacker
Francia
Dr Dorothée Leroux
Francia
Dr Isabella Vacchi
Francia
Dr Amélie Gavard
Francia
Caroline Wernert-Iberg
Francia
Test clinici
Setmelanotide (RM-493), Melanocortin-4 Receptor (MC4R) Agonist, in Bardet-BiedlSyndrome (BBS) and Alström Syndrome (AS) Patients With Moderate to Severe Obesity.
Argus® II Retinal Prosthesis System: Post-Market Study
Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci/Genes.
Bardet-Biedl Syndrome Study: Clinical and Genetic Epidemiology Study in Adults.
Clinical implication of Retinitis Pigmentosa molecular diagnostic using high throughput sequencing (RP-SEQ-HD).
Clinical Study of a single ciliopathy: Alström Syndrome.
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy.
Historical Case Record Survey of Visual Acuity Data From Patients With Leber’s Hereditary Optic Neuropathy (LHON).
Trisomy 21 in Adulthood : a medical and social situation in Alsace.
A double-masked, randomized, controlled, multiple-dose study to evaluate the efficacy, safety, tolerability and systemic exposure of QR-110 in Subjects with Leber’s Congenital Amaurosis (LCA) due to c.2991+1655A>G mutation (p.Cys998X) in the CEP290 gene (Illuminate).
Holistic Mixed Approaches to Capture the Real Life of Children With Rare Eye Diseases