Page last updated: 2024-10-26

ddt and Glycogen Storage Disease Type I

ddt has been researched along with Glycogen Storage Disease Type I in 1 studies

1,1-bis(p-chlorophenyl)-2,2,2-trichloroethane: structure in first source

Glycogen Storage Disease Type I: An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.

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
Sandifer, SH1

Other Studies

1 other study available for ddt and Glycogen Storage Disease Type I

ArticleYear
The susceptibility of the fetus and chils to chemical pollutants. Industrial and agricultural chemicals.
    Pediatrics, 1974, Volume: 53, Issue:5

    Topics: Adult; Agriculture; Atropine; Birth Weight; Black or African American; Blood; Body Burden; DDT; Envi

1974