#MPSVI
Today is the last #Naglazyme infusion of 2024. These weekly infusions have been occurring for over 20+ years. I’m so lucky that researchers took the time to work for a treatment for #Mucopolysaccharidosis Type VI. Feeling grateful.

#MPSVI #RareDisease #Disability #CareAboutRare
December 27, 2024 at 5:49 PM
ICYMI: Histopathological and Clinical-Genetic Analysis of Corneal Specimens in Maroteaux–Lamy Syndrome: Purpose:

Maroteaux–Lamy syndrome (MPSVI) is a rare lysosomal storage disorder caused by an Arylsulfatase B (ARSB) deficiency, leading to dermatan sulfate… #Cornea #Ophthalmology #Ophthotwitter
Histopathological and Clinical-Genetic Analysis of Corneal Specimens in Maroteaux–Lamy Syndrome
Purpose: Maroteaux–Lamy syndrome (MPSVI) is a rare lysosomal storage disorder caused by an Arylsulfatase B (ARSB) deficiency, leading to dermatan sulfate and chondroitin-4-sulfate accumulation. It manifests various systemic clinical features. Enzyme…
dlvr.it
March 16, 2025 at 10:09 AM
Histopathological and Clinical-Genetic Analysis of Corneal Specimens in Maroteaux–Lamy Syndrome: Purpose:

Maroteaux–Lamy syndrome (MPSVI) is a rare lysosomal storage disorder caused by an Arylsulfatase B (ARSB) deficiency, leading to dermatan sulfate and… #Cornea #Ophthalmology #Ophthotwitter
Histopathological and Clinical-Genetic Analysis of Corneal Specimens in Maroteaux–Lamy Syndrome
Purpose: Maroteaux–Lamy syndrome (MPSVI) is a rare lysosomal storage disorder caused by an Arylsulfatase B (ARSB) deficiency, leading to dermatan sulfate and chondroitin-4-sulfate accumulation. It manifests various systemic clinical features. Enzyme…
dlvr.it
March 14, 2025 at 10:08 AM