46,XY Differences of Sexual Development
- PMID: 25905393
- Bookshelf ID: NBK279170
46,XY Differences of Sexual Development
Excerpt
The 46,XY differences of sex development (46,XY DSD) can result either from decreased synthesis of testosterone and/or DHT or from impairment of androgen action. 46,XY DSD are characterized by micropenis, atypical or female external genitalia, caused by incomplete intrauterine masculinization with or without the presence of Müllerian structures. Male gonads are identified in the majority of 46,XY DSD patients, but in some of them no gonadal tissue is found. Complete absence of virilization results in normal female external genitalia and these patients generally seek medical attention at pubertal age, due to the absence of breast development and/or primary amenorrhea. A careful clinical evaluation of the neonate is essential because most DSD patients could be recognized in this period and prompt diagnosis allows a better therapeutic approach. Family and prenatal history, complete physical examination and assessment of genital anatomy are the first steps for a correct diagnosis. The diagnostic evaluation of DSD includes hormone measurements (assessment of Leydig and Sertoli cell function), imaging (ultrasonography is always the first and often the most valuable imaging modality in DSD patients’ investigation), cytogenetic, and molecular studies. Endoscopic and laparoscopic exploitation and/or gonadal biopsy are required in very few cases. Psychological evaluation is of crucial importance to treat DSD patients. Every couple that has a child with atypical genitalia must be assessed and receive counseling by an experienced psychologist, specialized in gender identity, who must act as soon as the diagnosis is suspected, and then follow the family periodically, more frequently during the periods before and after genitoplasty. Parents must be well informed by the physician and psychologist about normal sexual development. A simple, detailed, and comprehensive explanation about what to expect regarding integration in social life, sexual activity, need of hormonal and surgical treatment and the likely possibility or not of fertility according to the sex of rearing, should also be discussed with the parents before the assignment of final social sex. Optimal care of DSD patients begins in the newborn period and sometimes in prenatal life and requires a multidisciplinary team. Most of the well-treated DSD patients present a normal quality of life in adulthood. For complete coverage of all related areas of Endocrinology, please visit our on-line FREE web-text,
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Sections
- ABSTRACT
- INTRODUCTION
- INVESTIGATION OF DSD PATIENTS
- CYTOGENETIC AND MOLECULAR INVESTIGATION
- 46,XY DSD DUE TO ABNORMALITIES IN GONADAL DEVELOPMENT
- 46,XY DSD ASSOCIATED WITH CHOLESTEROL SYNTHESIS DEFECTS
- 46,XY DSD DUE TO TESTOSTERONE PRODUCTION DEFECTS
- 46,XY DSD DUE TO DEFECTS IN TESTOSTERONE METABOLISM
- 46,XY DSD DUE TO DEFECTS IN ANDROGEN ACTION
- 46,XY DSD DUE TO PERSISTENT MÜLLERIAN DUCT
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CONGENITAL NON -GENETIC 46,XY DSD - 46,XY OVOTESTICULAR DSD
- NON-CLASSIFIED FORMS
- GONADAL TUMOR DEVELOPMENT IN 46,XY DSD PATIENTS
- FERTILITY IN PATIENTS WITH 46,XY DSD
- 46,XY GENDER IDENTITY DISORDERS
- MANAGEMENT OF PATIENTS WITH 46,XY DSD
- ACKNOWLEDGMENT
- REFERENCES
References
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- Donahoe PK, Schnitzer JJ. Evaluation of the infant who has ambiguous genitalia, and principles of operative management. Semin Pediatr Surg. 1996;5(1):30–40. - PubMed
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- Sreenivasan R, Gonen N, Sinclair A. SOX Genes and Their Role in Disorders of Sex Development. Sex Dev. 2022:1–12. - PubMed
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- Pask A. The Reproductive System. Adv Exp Med Biol. 2016;886:1–12. - PubMed
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