formaldehyde has been researched along with Prader-Willi Syndrome in 1 studies
paraform: polymerized formaldehyde; RN given refers to parent cpd; used in root canal therapy
Prader-Willi Syndrome: An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Walczak, C | 1 |
Enders, H | 1 |
Grissinger, K | 1 |
Dufke, A | 1 |
1 other study available for formaldehyde and Prader-Willi Syndrome
Article | Year |
---|---|
Retrospective diagnosis of trisomy 15 in formalin-fixed, paraffin-embedded placental tissue in a newborn girl with Prader-Willi syndrome.
Topics: Adult; Amniocentesis; Chromosome Aberrations; Chromosomes, Human, Pair 15; Female; Formaldehyde; Hum | 2000 |