Other terms
Mucolipidosis,Type I Mucolipidosis,Mucolipidoses, Type I,Mucolipidosis, Type I,Type I Mucolipidoses,Mucolipidosis I,Mucolipidosis Is,Mucolipidosis Type 1,1, Mucolipidosis Type,1s, Mucolipidosis Type,Mucolipidosis Type 1s,Type 1, Mucolipidosis,Type 1s, Mucolipidosis,Myoclonus Cherry Red Spot Syndrome,Sialidosis,Sialidoses,Cherry Red Spot Myoclonus Syndrome,Mucolipidosis Type I,Mucolipidosis Type Is,Type III Mucolipidosis,Mucolipidoses, Type III,Mucolipidosis, Type III,Type III Mucolipidoses,Psuedo-Hurler Disease,Disease, Psuedo-Hurler,Diseases, Psuedo-Hurler,Psuedo Hurler Disease,Psuedo-Hurler Diseases,Pseudo-Hurler Polydystrophy,Polydystrophy, Pseudo-Hurler,Pseudo Hurler Polydystrophy,Mucolipidosis III,IIIs, Mucolipidosis,Mucolipidosis IIIs,Mucolipidosis Type III,Mucolipidosis Type IIIs,Type IV Mucolipidosis,Mucolipidoses, Type IV,Mucolipidosis, Type IV,Type IV Mucolipidoses,Mucolipidosis Type IV,Mucolipidosis Type IVs,Mucolipidosis IV,Mucolipidosis IVs,Deficiency Disease, Ganglioside Sialidase,Ganglioside Sialidase Deficiency Disease,Lipomucopolysaccharidosis,Lipomucopolysaccharidoses,Type II Mucolipidosis,Mucolipidoses, Type II,Mucolipidosis, Type II,Type II Mucolipidoses,Mucolipidosis Type II,Mucolipidosis Type IIs,Mucolipidosis II,Mucolipidosis IIs,I-Cell Disease,Disease, I-Cell,Diseases, I-Cell,I Cell Disease,I-Cell Diseases,Inclusion Cell Disease,Cell Disease, Inclusion,Cell Diseases, Inclusion,Disease, Inclusion Cell,Diseases, Inclusion Cell,Inclusion Cell Diseases
Description
Mucolipidoses: A group of inherited metabolic diseases characterized by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and mesenchymal cells. Abnormal amounts of sphingolipids or glycolipids are present in neural tissue. Mental retardation and skeletal changes, most notably dysostosis multiplex, occur frequently. (From Joynt, Clinical Neurology, 1992, Ch56, pp36-7)
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