The Izvestia News Center's press center talks about modern approaches to early detection of orphan pathologies. Broadcast

A press conference on "Early diagnosis of rare diseases: alertness, algorithms, technologies" is being held at the Izvestia News Center.

They talk about early clinical markers that make it possible to suspect a rare disease at the initial stage, about modern diagnostic methods and improving the care system for patients with orphan diseases.:

- Nato Vashakmadze, MD, Professor of the Department of Faculty Pediatrics at the Institute of Motherhood and Childhood of the Pirogov Russian National Research Medical University, Head of the Department of Orphan Diseases and the Prevention of Disabling Diseases at the Institute of Pediatrics and Child Health NCC No. 2 of the Russian National Research Medical Center. Academician of B.V. Petrovsky";

- Sergey Bochenkov, geneticist, Head of the Pediatric Department of Congenital and Hereditary Diseases of the Yu.E. Veltischev Institute of Pediatrics and Pediatric Surgery of the Pirogov Russian National Research Medical University of the Ministry of Health of the Russian Federation;

- Tatiana Strokova, MD, Professor of the Russian Academy of Sciences, Head of the Department of Pediatric Gastroenterology, Hepatology and Dietotherapy at the Federal State Budgetary Institution "FIT Nutrition and Biotechnology", Head of the Department of Gastroenterology and Dietetics at the Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation;

- Sofia Popovich, neurologist, researcher at the Center for Pediatric Neuropsychiatry of the Federal State Budgetary Educational Institution "NMIC of Children's Health" of the Ministry of Health of the Russian Federation.

Moderator — Ekaterina Zakharova, MD, Associate Professor, Head of the Laboratory of Hereditary Metabolic Diseases of the Federal State Budgetary Budgetary Institution "MGNC", Director of the ANO INBO OMICS, Chairman of the Expert Council of the All-Russian Society of Rare (Orphan) Diseases.