estriol has been researched along with Zellweger Syndrome in 2 studies
hormonin: estrogen replacement; each tablet contains 600 ug micronized 17beta-estradiol, 270 ug estriol and 1.4 mg estrone
chlorapatite : A phosphate mineral with the formula Ca5(PO4)3Cl.
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 | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
de Graaf, IM | 1 |
Pajkrt, E | 1 |
Keessen, M | 1 |
Leschot, NJ | 1 |
Bilardo, CM | 1 |
Johnson, JM | 1 |
Babul-Hirji, R | 1 |
Chitayat, D | 1 |
2 other studies available for estriol and Zellweger Syndrome
Article | Year |
---|---|
Enlarged nuchal translucency and low serum protein concentrations as possible markers for Zellweger syndrome.
Topics: Adult; alpha-Fetoproteins; Biomarkers; Cesarean Section; Chorionic Gonadotropin; Estriol; Fatal Outc | 1999 |
First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome.
Topics: Adult; Diagnosis, Differential; Estriol; Female; Humans; Hypokinesia; Neck; Pregnancy; Pregnancy Out | 2001 |