glycine has been researched along with Zellweger Syndrome in 2 studies
Zellweger Syndrome: An autosomal recessive disorder due to defects in PEROXISOME biogenesis which involves more than 13 genes encoding peroxin proteins of the peroxisomal membrane and matrix. Zellweger syndrome is typically seen in the neonatal period with features such as dysmorphic skull; MUSCLE HYPOTONIA; SENSORINEURAL HEARING LOSS; visual compromise; SEIZURES; progressive degeneration of the KIDNEYS and the LIVER. Zellweger-like syndrome refers to phenotypes resembling the neonatal Zellweger syndrome but seen in children or adults with apparently intact peroxisome biogenesis.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 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 |
|---|---|
| Gärtner, J | 1 |
| Preuss, N | 1 |
| Brosius, U | 1 |
| Biermanns, M | 1 |
| Libert, R | 1 |
| Hermans, D | 1 |
| Draye, JP | 1 |
| Van Hoof, F | 1 |
| Sokal, E | 1 |
| de Hoffmann, E | 1 |
2 other studies available for glycine and Zellweger Syndrome
| Article | Year |
|---|---|
Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype.
Topics: Aspartic Acid; ATPases Associated with Diverse Cellular Activities; Child; Glycine; Humans; Infant; | 1999 |
Bile acids and conjugates identified in metabolic disorders by fast atom bombardment and tandem mass spectrometry.
Topics: Adrenoleukodystrophy; Bile Acids and Salts; Glycine; Humans; Hydroxylation; Mass Spectrometry; Metab | 1991 |