Hurler Syndrome/MPS 1: Parents talk about getting through and staying present

New book teaches about life with Hurler's Syndrome

Courtagen Many Faces of Mitochondrial Disorders

Генная терапия у детей с МПС I показывает многообещающие результаты

Parent Vlogs: Our MPS I Diagnostic Journey

Local family shares experience with rare Angelman Syndrome

Я ВСЕГДА БЫЛ ЭКСПОНАТОМ ДЛЯ СТУДЕНТОВ МЕДИКОВ. Синдром Марфана

The Ladd Family - Our Journey with MPS 1 Hurler Syndrome- Ep.1

Teen Battling Sanfilippo Syndrome, aka ‘Childhood Alzheimer's’

Hurler Syndrome/MPS 1: Parents talk about their brave boy post stem cell transplant.

Meet Nathan—Mitochondrial Disease Patient

One: MPS 1 Diagnosis

Overview of Mucopolysaccharidoses with a Science Twist

Жизнь с гипермобильным синдромом Элерса-Данлоса + наши средства передвижения при участии Мартины

Raising awareness around Leigh Syndrome

Любовь для Лолы (синдром Аперта)

Behind the Mystery of Gaucher Disease

What is Hunter syndrome? (MPS II)

Как жить со СМА - спинальная мышечная атрофия | Kssyaomi

Fragile X Syndrome (FXS) 10 Things You Did Not Know

Subtle Symptoms of a Rare Disease – Mucopolysaccharidosis I (MPS I)