Rare diseases | PMNET Forum 2026

Chair: Madara Auzenbaha, Lina Jankaskaite Speaker: Kristīne Rasnača Chair, Latvian Society of Neonatology; Lecturer, Department of Pediatrics, Rīga Stradiņš University, Latvia Talk: Genome-wide DNA methylation analysis reveals focal epigenetic dysregulation in small-for-gestational-age placentas and its potential links to rare syndromes Speaker: Liuda Brogiene, Lithuanian University Of Health Sciences, Kaunas, Lithuania Talk: Chronic Pain in Rare Diseases: The Role of Precision Medicine Speaker: Vladimirs Krutovs Neurologist, Pauls Stradiņš Clinical University Hospital, Latvia Talk: Improving the Patient Journey in Myasthenia Gravis: From Diagnosis to Long-Term Care Speaker: Lina Jankauskaite, Lithuanian University Of Health Sciences, Kaunas, Lithuania Talk: Counting the stripes: turning rare disease data into personalized care