A case of SRY Negative 46, XX Male Syndrome with Deletion on Long Arm of X Chromosome.
- Author:
Ji Woong LEE
1
;
Chang Hee HONG
;
Hye Ran KIM
;
Jong Beom SIN
Author Information
1. Department of Pediatrics, College of Medicine, Inje University, Busan, Korea. pedsin@inje.ac.kr
- Publication Type:Case Report
- Keywords:
XX male;
Ambiguous genitalia;
Sex-determining region of Y (SRY)
- MeSH:
46, XX Testicular Disorders of Sex Development*;
Arm*;
Disorders of Sex Development;
Genitalia;
Humans;
Incidence;
Infant, Newborn;
Male;
Parturition;
Penis;
Testis;
X Chromosome*;
Y Chromosome
- From:Korean Journal of Perinatology
2006;17(3):353-358
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
46,XX male sex reversal syndrome is, also called the de la Chapelle syndrome, a rare cause of abnormal sex determination with an incidence of 1 in 20,000~25,000 male neonates. The condition of 46,XX is characterized by testicular development in subject who have two X chromosomes but who lack a normal Y chromosome. All patients have small and azospermic testes and no evidence of ovarian tissue or Mullerian duct derivatives. XX males can be classified as Y positive or Y negative, depending on the presence or absence of Y specific sequences. SRY positive XX male have normal genitalia with a small penis, however, 10~15% of patients are SRY negative XX male, exhibit various degrees of genital ambiguity and can be diagnosed at birth or during early childhood. We experienced a case of sex determining region on the Y chromosome (SRY) negative 46,XX male syndrome neonate, with deletion on the long arm of X chromosome.
