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Дефіцит гіалуронідази

ORPHA:67041· ICD-10 E76.2· Hyaluronidase deficiency

Визначення(English summary)

A 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).

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Childhood