chondroitin and Hypertrichosis

chondroitin has been researched along with Hypertrichosis* in 5 studies

Reviews

1 review(s) available for chondroitin and Hypertrichosis

ArticleYear
The systemic mucopolysaccharidoses.
    Ergebnisse der inneren Medizin und Kinderheilkunde, 1972, Volume: 32

    Topics: Adolescent; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Chondroitin; Chromosome Aberrations; Chromosome Disorders; Female; Fetus; Glycolipids; Glycosaminoglycans; Humans; Hypertrichosis; Infant; Intellectual Disability; Joint Diseases; Male; Microscopy, Electron; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa

1972

Other Studies

4 other study(ies) available for chondroitin and Hypertrichosis

ArticleYear
Chemical definition of the mucopolysaccharidoses.
    Clinica chimica acta; international journal of clinical chemistry, 1975, Mar-24, Volume: 59, Issue:3

    Glycosaminoglycans were isolated from the urines of 46 patients with mucopolysaccharidosis; 11 with Type I (Hurler), 8 with Type II (Hunter), 16 with Type III (Sanfilippo A and B), 9 with Type V (Scheie), one with Type VI (Marateaux-Lamy), and one unclassified. All 46 patients excreted in their urine excessive amounts of dermatan sulfate, heparan sulfate or both. In addition, patients of certain types excreted excessive amounts of chondroitin sulfates A and/or C. There is a trend in each type of the disease towards the same carbazole/orcinol ratio, glucosamine/galactosamine ratio and glycosaminoglycan composition. Molecular weight distribution of the urinary glycosaminoglycans by gel filtration from Sephadex G-200 is characteristic for each different type of mucopolysaccharidosis and is distinguished from normal controls and patients without mucopolysaccharidosis. Preparation of elution diagrams from Sephadex G-200 allows an estimation of the composition of the glycosamino-glycans. Practically all heparan sulfate and a sizable part of dermatan sulfate from the urinary glycosaminoglycans of all these patients have been highly degraded. In all the patients in which the specific enzyme defect was demonstrated, the assignment of the type of mucopolysaccharidosis, on the basis of the elution diagrams, was correct. Patients with mucopolysaccharidosis Type V displayed two conspicuously different types of elution patterns, suggesting heterogeneity. Indeed, only a portion of these patients showed alpha-L- iduronidase deficiency. Carriers had normal urinary glycosaminoglycan output and composition and exhibited normal elution diagrams.

    Topics: Adolescent; Adult; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Dermatan Sulfate; Female; Glycosaminoglycans; Heparitin Sulfate; Humans; Hypertrichosis; Infant; Intellectual Disability; Joint Diseases; Male; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Retinitis Pigmentosa

1975
[Diagnosis of hereditary mucopolysaccharidoses].
    Nihon Hifuka Gakkai zasshi. The Japanese journal of dermatology, 1972, Volume: 82, Issue:9

    Topics: Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography; Chromosome Aberrations; Chromosome Disorders; Glycosaminoglycans; Humans; Hypertrichosis; Intellectual Disability; Joint Diseases; Mucopolysaccharidoses; Retinitis Pigmentosa

1972
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
    Biochemical medicine, 1970, Volume: 3, Issue:5

    Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glutamates; Glycine; Glycosaminoglycans; Humans; Hypertrichosis; Joint Diseases; Male; Mucopolysaccharidosis I; Retinitis Pigmentosa; Serine; Uronic Acids

1970
A new mucopolysaccharidosis.
    The Journal of pediatrics, 1970, Volume: 77, Issue:2

    Topics: Adolescent; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Chondroitin; Corneal Opacity; Female; Heparin; Humans; Hypertrichosis; Intellectual Disability; Joint Diseases; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa

1970