Add to ORKGFive cats with feline α-L-iduronidase-deficient mucopolysaccharidosis were studied. Membrane-bound cytoplasmic inclusions were present in central nervous system neurons, hepatocytes, chondrocytes, vascular and splenic smooth muscle cells, bone marrow leukocytes, and fibroblasts of the skin, eye, and cardiac valves. The lesions in these cats closely resemble those described in human patients with mucopolysaccharidosis I H (Hurler syndrome)
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI), a lysosomal storage disease, is one of the more prevalent in...
Abstract Background Mucolipidosis II (ML II; I-cell disease) is caused by a deficiency of N-acetylgl...
Three cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and tra...
Five cats with feline α-L-iduronidase-deficient mucopolysaccharidosis were studied. Membrane-bound c...
Abstract. Mucopolysaccharidosis VII was diagnosed in a domestic shorthair cat from California. The c...
Abstract. A 7-month-old female cat was seen for abnormal facial features and abnormality of gait. Fa...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Abstract. A male cat 12-1 4 weeks old had walking difficulties and an enlarged abdomen. Facial dysmo...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
Severe mucopolysaccharidosis type I (MPS I) is a fatal neuropathic lysosomal storage disorder with s...
A 3-year-old Siamese/short-haired European cat was referred for clinical disease characterized by dw...
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI), a lysosomal storage disease, is one of the more prevalent in...
Abstract Background Mucolipidosis II (ML II; I-cell disease) is caused by a deficiency of N-acetylgl...
Three cats with feline arylsulfatase-B-deficient mucopolysaccharidosis were studied by light and tra...
Five cats with feline α-L-iduronidase-deficient mucopolysaccharidosis were studied. Membrane-bound c...
Abstract. Mucopolysaccharidosis VII was diagnosed in a domestic shorthair cat from California. The c...
Abstract. A 7-month-old female cat was seen for abnormal facial features and abnormality of gait. Fa...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Abstract. A male cat 12-1 4 weeks old had walking difficulties and an enlarged abdomen. Facial dysmo...
Two long-haired Siamese cats are reported with clinical manifestations of human mucopolysaccharidosi...
Mucolipidosis II (ML II), also called I-cell disease, is a unique lysosomal storage disease caused b...
Severe mucopolysaccharidosis type I (MPS I) is a fatal neuropathic lysosomal storage disorder with s...
A 3-year-old Siamese/short-haired European cat was referred for clinical disease characterized by dw...
Mucopolysaccharidosis type VI (MPS VI) is a lysosomal storage disease caused by a deficiency of N-ac...
Mucopolysaccharidosis type VI (MPS VI), a lysosomal storage disease, is one of the more prevalent in...
Abstract Background Mucolipidosis II (ML II; I-cell disease) is caused by a deficiency of N-acetylgl...