Analysis of HPRT1 gene variant and prenatal diagnosis for a Chinese pedigree with Lesch-Nyhan syndrome but no specimen from affected probands.
10.3760/cma.j.cn511374-20211029-00861
- Author:
Ming TONG
1
;
Qian LI
;
Anping SUN
;
Canming CHEN
;
Suwei HU
Author Information
1. Medical Genetic Center, Yangzhou Maternal and Child Health Care Hospital, the Affiliated Hospital of Yangzhou University Medical College, Yangzhou, Jiangsu 225002, China. husuwei2004@126.com.
- Publication Type:Journal Article
- MeSH:
Male;
Female;
Humans;
Pregnancy;
Lesch-Nyhan Syndrome/genetics*;
Pedigree;
Hypoxanthine Phosphoribosyltransferase/genetics*;
Prenatal Diagnosis;
China;
Mutation
- From:
Chinese Journal of Medical Genetics
2022;39(11):1243-1246
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To carry out genetic testing and prenatal diagnosis for a Chinese pedigree with Lesch-Nyhan syndrome (LNS) but no specimen from the affected probands.
METHODS:All affected individuals in this pedigrees were male and had deceased during childhood, with no biological specimen left. Based on their typical neurological dysfunction and tendency for self-mutilation, the diagnosis of LNS was suspected. Sanger sequencing was carried out to detect potential variant of the HPRT1 gene among female members from the pedigree. Following the identification of the pathogenic variant, prenatal diagnosis was provided for a high-risk fetus.
RESULTS:The proband's mother and three other females were found to harbor heterozygous c.500_501delGGinsC (p.Arg167fs*23) variant of the HPRT1 gene, which was unreported previously. Prenatal diagnosis showed that the fetus was a male and had inherited the same pathogenic variant.
CONCLUSION:The c.500_501delGGinsC variant of the HPRT1 gene probably underlay the LNS in this pedigree. Above finding has provided a basis for prenatal diagnosis and genetic counseling for this pedigree.
