mucoid degeneration n.
The degeneration of connective tissue into a gelatinous or mucoid substance.
mucolipidosis mu·co·lip·i·do·sis (myōō’kō-lĭp’ĭ-dō’sĭs) n. Any of a group of hereditary metabolic storage diseases resembling Hurler’s syndrome but with normal urinary mucopolysaccharides.
- Mucolipidosis i
mucolipidosis I n. Mucolipidosis having symptoms resembling those of Hurler’s syndrome but milder, and with moderate mental retardation. Also called lipomucopolysaccharidosis.
- Mucolipidosis ii
mucolipidosis II n. Mucolipidosis characterized by symptoms resembling those of Hurler’s syndrome but more severe, with normal levels of urinary mucopolysaccharides and the presence of inclusion bodies in cultured fibroblasts. Also called inclusion cell disease.
- Mucolipidosis iii
mucolipidosis III n. Mucolipidosis characterized by symptoms resembling those of Hurler’s syndrome, but milder, with restricted joint mobility, short stature, mild mental retardation, and dysplastic skeletal changes.