Page last updated: 2024-10-17

chlorine and Mucopolysaccharidosis I

chlorine has been researched along with Mucopolysaccharidosis I in 2 studies

chloride : A halide anion formed when chlorine picks up an electron to form an an anion.

Mucopolysaccharidosis I: Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hopwood, JJ1
Muller, V1
Manley, G1
Hawksworth, J1

Other Studies

2 other studies available for chlorine and Mucopolysaccharidosis I

ArticleYear
Biochemical discrimination of Hurler and Scheie syndromes.
    Clinical science (London, England : 1979), 1979, Volume: 57, Issue:3

    Topics: Child; Chlorides; Fibroblasts; Glucaric Acid; Glucuronidase; Humans; Hydrogen-Ion Concentration; Hyd

1979
Diagnosis of Hurler's syndrome in the hospital laboratory and the determination of its genetic type.
    Archives of disease in childhood, 1966, Volume: 41, Issue:215

    Topics: Chlorides; Electrophoresis; Glycosaminoglycans; Humans; In Vitro Techniques; Infant, Newborn; Mucopo

1966