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🔗 CustomizeMedical Overview of Deficiency Of Hyaluronoglucosaminidase
Sources citedA rare form of mucopolysaccharidosis characterized by abnormal storage of hyaluronan in lysosomes due to deficiency of hyaluronidase 1. Clinical manifestations include knee and/or hip pain associated with swelling, diffuse joint involvement with proliferative synovitis and occurrence of multiple periarticular soft-tissue masses, short stature, and dysmorphic craniofacial features (such as flattened nasal bridge, bifid uvula, and cleft palate).
Classification & codes: GARD 0016675 · Orphanet ORPHA:67041 · OMIM 601492 · ICD-10 E76.2
Sources: GARD (NIH/NCATS), Orphanet · last reviewed 2026. Educational only — not medical advice.
News & Updates
ALYFTREK shows positive Phase 3 results in children ages 2–5
Vertex plans global regulatory submissions for this pediatric age group in the first half of 2026.
Airway clearance routines that actually work for teens
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Care & management overview — Deficiency Of Hyaluronoglucosaminidase
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Deficiency Of Hyaluronoglucosaminidase News & Developments
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Disclosure, accommodations, insurance transitions and workplace planning for teens and young adults with MPS9.
Sources: GARD (NIH/NCATS), Orphanet · last reviewed 2026. Educational only — not medical advice.