Mucopolysaccharidosis type 4
MONDO:0018938A lysosomal storage disease belonging to the group of mucopolysaccharidoses, and characterized by spondylo-epiphyso-metaphyseal dysplasia. It exists in two forms, A and B.
Also known as: MPS4, MPSIV, Morquio disease, Morquio syndrome, Mucopolysaccharidosis IV, eccentro-osteochondrodysplasia, eccentrochondrodysplasia, eccentroosteochondrodysplasia
13 clinical trials for this condition and its sub-types, 2 tagged with Mucopolysaccharidosis type 4 itself.
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Browse by category →Sub-types of Mucopolysaccharidosis type 4
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Mucopolysaccharidosis type 4A 8 trials
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Morquio syndrome C 0 trials
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Mucopolysaccharidosis type 4B 0 trials
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Massive french study aims to unlock secrets of rare MPS diseases
Knowledge-focused Recruiting nowThis observational study will follow up to 1,000 people in France with mucopolysaccharidosis (MPS), a group of rare genetic disorders. Researchers will collect medical data from patient records and ongoing checkups to map how the diseases progress and how current treatments affec…
Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:05 UTC
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Major study tracks rare brain diseases to unlock their secrets
Knowledge-focused Recruiting nowThis study follows 1500 people with rare genetic brain disorders to learn how these diseases progress. Researchers measure thinking, movement, and daily living skills over time, and also look at brain scans and body fluids. The goal is to better understand the diseases and how tr…
Sponsor: University of Pittsburgh • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:03 UTC