Progress in genetics of Prader-Willi syndrome
10.3760/cma.j.cn101070-20190526-00451
- VernacularTitle:Prader-Willi综合征的遗传学研究进展
- Author:
Xiaohong CHEN
;
Lifang FENG
;
Hui YAO
- From:
Chinese Journal of Applied Clinical Pediatrics
2021;36(1):77-80
- CountryChina
- Language:Chinese
-
Abstract:
Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused by the lack of expression of genes associated with the 15q11.2-q13 region of the paternal chromosome.There are three main types of genetic mechanisms, deletion of the paternal critical region, maternal uniparental disomy and imprinting center defect.Genetic counseling can be carried out based on different genetic mechanisms of PWS, both re-fertility assessments and prenatal diagnoses were performed on couples whose children have already had the disease.The pathogeny and mechanism of PWS are complex.The rapid development of molecular genetics and related research have provided a basis for further understanding of this disease.In this paper, the advances in the genetics of PWS were reviewed.
