Genetic analysis of a case of 46, XX, SRY－ male syndrome.
- Author:
Ren WANG
1
Author Information
- Publication Type:Case Reports
- Keywords: 46,XX male syndrome; single nucleotide polymorphism (SNP) array
- MeSH: 46, XX Testicular Disorders of Sex Development; diagnosis; genetics; Chromosome Aberrations; Chromosome Banding; Genetic Testing; Humans; Infertility, Male; genetics; Karyotype; Karyotyping; Male; Phenotype; Sex-Determining Region Y Protein; genetics
- From: National Journal of Andrology 2018;24(5):431-435
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo identify the etiology of chromosome abnormality in an infertile man and analyze the correlation between the genotype and phenotype.
METHODSWe analyzed the karyotype of an infertile male using the routine G-banding technique and then the chromosome abnormality of the patient by Illumina Human CytoSNP-12 Beadchip array.
RESULTSNegative results were found in the examination of the sex-determining region Y (SRY) gene and the STR locus in the AZF zone of the patient. The karyotype of the patient was 46, XX. SNP array showed a 1.05 Mb 19p12 duplication and a 0.93 Mb Xq27.1 duplication.
CONCLUSIONSThe patient was confirmed as a case of 46,XX male syndrome. The increased copies of the FGF13 gene may be the major causes of abnormal sex determination and testis development.
