Publications by authors named "Jiena Fu"
[Analysis of prenatal phenotype and pathogenetic variant in a fetus with Papillorenal syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
September 2020
Article Synopsis
- A study was conducted on 53,873 newborns in Zhengzhou to determine the prevalence of genetic variants related to deafness.
- Out of the newborns tested, 2,770 were found to carry deafness-related variants, resulting in a carrier rate of 5.142%. The most common gene variants identified were in GJB2 and SLC26A4.
- The findings emphasize the importance of early genetic screening for deafness to facilitate timely diagnosis and treatment for affected infants.
Objective: To search the mechanism of Huaisanzhen in treating the nerve root pain caused by protrusion of lumbar intervertebra disc.
Methods: Sixty male SD rats were randomly divided into a normal control group, a sham operation control group, a model control group, an aspirin-DL-lysine control group, a routine body acupuncture group, and a Huaisanzhen treatment group. The aspirin-DL-lysine control group, the routine body acupuncture group and the Huaisanzhen treatment group were treated by aspirin-DL-lysine through intramuscular injection, routine acupuncture and Huaisanzhen therapy, respectively.