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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hopwood, JJ | 1 |
| Muller, V | 1 |
| Manley, G | 1 |
| Hawksworth, J | 1 |
2 other studies available for chlorine and Mucopolysaccharidosis I
| Article | Year |
|---|---|
Biochemical discrimination of Hurler and Scheie syndromes.
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.
Topics: Chlorides; Electrophoresis; Glycosaminoglycans; Humans; In Vitro Techniques; Infant, Newborn; Mucopo | 1966 |