Nomura Y, Yagi H, Onigata K, Yutani S, Nagashima T, Ogawa R, Nagashima K, Morikawa A
Department of Pediatrics, Gunma University School of Medicine, Japan.
Acta Paediatr Jpn. 1995 Dec;37(6):706-9. doi: 10.1111/j.1442-200x.1995.tb03410.x.
The unusual case of a Japanese newborn XX male is presented. Examination of chromosomes in amniotic fluid cells had shown a normal female karyotype (46,XX), but ultrasonography revealed a penis and a scrotum. The neonate had normal male external genitalia, and serum levels of luteinizing hormone, follicle stimulating hormone, and testosterone were all within the normal range. High resonance chromosome analysis revealed an excess portion on the short arm of one of the X chromosomes. We examined his genomic DNA by polymerase chain reaction (PCR) and detected two Y specific regions in his genomic DNA, the sex-determining region Y (SRY) and pseudoautosomal boundary Y. Nucleotide sequencing of the PCR products of SRY indicated no mutation. These findings suggested that the translocation or insertion of an SRY region on the X chromosome led to the development of testicles and a male phenotype.
