Page last updated: 2024-10-20

sulfites and Down Syndrome

sulfites has been researched along with Down Syndrome in 4 studies

Sulfites: Inorganic salts of sulfurous acid.
sulfites : Any sulfurous acid derivative that is a salt or an ester of sulfurous acid.
organosulfonate oxoanion : An organic anion obtained by deprotonation of the sufonate group(s) of any organosulfonic acid.
sulfite : A sulfur oxoanion that is the conjugate base of hydrogen sulfite (H2SO3).

Down Syndrome: A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Laufer, BI1
Hwang, H1
Jianu, JM1
Mordaunt, CE1
Korf, IF1
Hertz-Picciotto, I1
LaSalle, JM1
Lun, FM1
Chiu, RW1
Sun, K1
Leung, TY1
Jiang, P1
Chan, KC1
Sun, H1
Lo, YM1
Yin, YZ1
She, Q1
Zhang, J1
Zhang, PZ1
Zhang, Y1
Lin, JW1
Ye, YC1
Kerkel, K1
Schupf, N1
Hatta, K1
Pang, D1
Salas, M1
Kratz, A1
Minden, M1
Murty, V1
Zigman, WB1
Mayeux, RP1
Jenkins, EC1
Torkamani, A1
Schork, NJ1
Silverman, W1
Croy, BA1
Tycko, B1

Other Studies

4 other studies available for sulfites and Down Syndrome

ArticleYear
Low-pass whole genome bisulfite sequencing of neonatal dried blood spots identifies a role for RUNX1 in Down syndrome DNA methylation profiles.
    Human molecular genetics, 2021, 01-06, Volume: 29, Issue:21

    Topics: Biomarkers; Case-Control Studies; Core Binding Factor Alpha 2 Subunit; CpG Islands; DNA Methylation;

2021
Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA.
    Clinical chemistry, 2013, Volume: 59, Issue:11

    Topics: Chromosomes, Human, Pair 21; DNA; DNA Methylation; Down Syndrome; Epigenesis, Genetic; Female; Fetus

2013
Placental methylation markers in normal and trisomy 21 tissues.
    Prenatal diagnosis, 2014, Volume: 34, Issue:1

    Topics: Chromosomes, Human, Pair 21; DNA; DNA Methylation; Down Syndrome; Epigenesis, Genetic; Female; Genet

2014
Altered DNA methylation in leukocytes with trisomy 21.
    PLoS genetics, 2010, Nov-18, Volume: 6, Issue:11

    Topics: Adult; Aging; Azacitidine; Child; Child, Preschool; DNA Methylation; Down Syndrome; Gene Expression

2010