Genetic heterogeneity within the chondroitinsulphaturias.

The approach, identification of clinical phenotype followed by lysosomal enzyme assays in cell culture, used in the classification of the genetic mucopolysaccharidoses I-VI has been applied to the chondroitinsulphaturias. There was evidence of heterogeneity in the first 9 patients reported.

[1]  R. Stevenson,et al.  The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features. , 1976, Pediatrics.

[2]  D. Rimoin,et al.  PHENOTYPIC VARIATION IN ALPHA-L-IDURONIDASE DEFICIENCY , 1975, The Lancet.

[3]  W. Sly,et al.  β-Glucuronidase deficiency mucopolysaccharidosis , 1975 .

[4]  R. Stephens Letter: Splenectomy and lymphomas. , 1975, Lancet.

[5]  J. Spranger,et al.  CHONDROITINSULPHATURIA WITH α-L-IDURONIDASE DEFICIENCY , 1974 .

[6]  M. Dean,et al.  CHONDROITINSULPHATURIA WITH α-L-IDURONIDASE DEFICIENCY , 1974 .

[7]  J. Hansky Letter: Antral-gastrin-cell hyperplasia in peptic ulcer disease. , 1974, Lancet.

[8]  Neufeld Ef The biochemical basis for mucopolysaccharidoses and mucolipidoses. , 1974 .

[9]  W. Horton,et al.  Chondroitin-6-sulfate mucopoly-saccharidosis in conjunction with lymphopenia, defective cellular immunity and the nephrotic syndrome. , 1974, Birth defects original article series.

[10]  E. Neufeld The biochemical basis for mucopolysaccharidoses and mucolipidoses. , 1974, Progress in medical genetics.

[11]  B. Danes,et al.  Chondroitin-6-sulfate mucopolysaccharidosis in conjuntion withlymphopenia, defective cellular immunity and the nephrotic syndrome. , 1974, Birth defects original article series.

[12]  W. Sly,et al.  Beta-glucuronidase deficiency mucopolysaccharidosis. , 1974, Birth defects original article series.

[13]  A. Beaudet,et al.  Beta-glucuronidase deficiency (mucopolysaccharidosis type VII). , 1974, Birth defects original article series.

[14]  O. Kolar SUBACUTE SCLEROSING PANENCEPHALITIS AND SALK VACCINE , 1973 .

[15]  B. Danes,et al.  Mucopolysaccharides in Urine during Normal Human Development , 1973, Pediatric Research.

[16]  W. Sly,et al.  Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis. , 1973, The Journal of pediatrics.

[17]  A. Bearn,et al.  THE HURLER SYNDROME: A STUDY OF CULTURED LYMPHOID CELL LINES , 1972, The Journal of experimental medicine.

[18]  M. Dean,et al.  A Form of Mucopolysaccharidosis with Visceral Storage and Excessive Urinary Excretion of Chondroitin Sulphate , 1972, Developmental medicine and child neurology.

[19]  Victor A. McKusick,et al.  Heritable disorders of connective tissue , 1972 .

[20]  G. Thompson,et al.  A mucopolysaccharidosis with increased urinary excretion of chondroitin-4 sulfate. , 1971, Annals of internal medicine.

[21]  F. Freitag,et al.  Chondroitin-4-sulfate mucopolysaccharidosis. , 1971, Helvetica paediatrica acta.

[22]  J. Onisawa,et al.  Chondroitin 4- and 6-sulfaturia in Morquio-Ullrich's syndrome. , 1971, Biochemical medicine.

[23]  M. Philippart,et al.  Chondroitin-4-sulphate mucopolysaccharidosis--a new variant of Hurler's syndrome. , 1969, Lancet.

[24]  V. Näntö,et al.  Transplantation of Tissues, Vol. II , 1960 .

[25]  A. G. Steinberg,et al.  Progress in Medical Genetics , 1970 .