Mucopolysaccharidoses (MPS) | Genetic Disorders Lecture Series 2025

Welcome to our **Biochemistry and Pathology Course Series**!
In this lecture, we discuss **Mucopolysaccharidoses (MPS)** — a group of **inherited lysosomal storage disorders** caused by **enzyme deficiencies** that impair the degradation of **glycosaminoglycans (GAGs)** such as heparan sulfate and dermatan sulfate.

📚 **Topics Covered:**
🔹 Definition & Biochemical Basis of MPS
🔹 Enzyme Deficiencies and Accumulated Substrates
🔹 Types of MPS (I to VII) – Hurler, Hunter, Sanfilippo, Morquio, and more
🔹 Clinical Features – Coarse facial features, organomegaly, skeletal deformities, corneal clouding, mental retardation
🔹 Diagnostic Methods – Enzyme assays, urine tests, genetic analysis
🔹 Management & Recent Advances – Enzyme replacement therapy, gene therapy, supportive care

👨‍⚕️ Ideal for **MBBS, MD Biochemistry, and Pathology students** who want a clear understanding of **genetic metabolic disorders** with a clinical and molecular perspective.

Disclaimer:**

This lecture is created **for educational and academic purposes only** 🩺.
It is intended for **medical students, residents, and healthcare professionals** to enhance their understanding of **Mucopolysaccharidoses and related metabolic disorders**.
The information provided here **should not be used as medical advice or for patient treatment**.
Always consult a qualified healthcare provider for clinical decisions.
All visuals, animations, and examples are used **for teaching and demonstration only**.
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Видео Mucopolysaccharidoses (MPS) | Genetic Disorders Lecture Series 2025 канала LecturePoint