Page last updated: 2024-11-06

mitomycin and Prader-Willi Syndrome

mitomycin has been researched along with Prader-Willi Syndrome in 1 studies

Mitomycin: An antineoplastic antibiotic produced by Streptomyces caespitosus. It is one of the bi- or tri-functional ALKYLATING AGENTS causing cross-linking of DNA and inhibition of DNA synthesis.
mitomycin : A family of aziridine-containing natural products isolated from Streptomyces caespitosus or Streptomyces lavendulae.

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)

Research Excerpts

ExcerptRelevanceReference
"Analysis of chromosome breakage with mitomycin C (MMC) and folate-deficient culture conditions was undertaken on 18 Prader-Labhart-Willi syndrome (PLWS) patients (10 with 15q12 deletion [5 females, 5 males; mean age = 17."3.67Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome. ( Butler, MG; Jenkins, BB, 1989)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Butler, MG1
Jenkins, BB1

Other Studies

1 other study available for mitomycin and Prader-Willi Syndrome

ArticleYear
Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome.
    American journal of medical genetics, 1989, Volume: 32, Issue:4

    Topics: Adolescent; Adult; Cells, Cultured; Child; Child, Preschool; Chromosome Deletion; Chromosome Fragile

1989