The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17 beta-hydroxysteroid-dehydrogenase type 3 enzyme deficiency

被引:7
|
作者
Costa, Carla [1 ]
Castro-Correia, Cintia [1 ]
Mira-Coelho, Alda [2 ]
Monteiro, Bessa [3 ]
Monteiro, Joaquim [3 ]
Hughes, Ieuan [4 ]
Fontoura, Manuel [1 ]
机构
[1] Hosp Sao Joao, Fac Med Porto, Dept Paediat, Paediat Endocrinol & Diabetol Unit, Alameda Prof Hernani Monteiro, P-4202451 Oporto, Portugal
[2] Hosp Sao Joao, Dept Psychiat, Oporto, Portugal
[3] Hosp Sao Joao, Dept Paediat Surg, Oporto, Portugal
[4] Univ Cambridge, Addenbrookes Hosp, Dept Paediat, Endocrinol & Diabetol Unit, Cambridge, England
关键词
D O I
10.1530/EDM-14-0064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The development of male internal and external genitalia in an XY fetus requires a complex interplay of many critical genes, enzymes, and cofactors. The enzyme 17 beta-hydroxysteroid-dehydrogenase type 3 (17 beta HSD3) is present almost exclusively in the testicles and converts Delta 4-androstenodione (Delta 4) to testosterone. A deficiency in this enzyme is rare and is a frequently misdiagnosed autosomal recessive cause of 46, XY, disorder of sex development. The case report is of a 15-year-old adolescent, who was raised according to female gender. At puberty, the adolescent had a severe virilization and primary amenorrhea. The physical examination showed a male phenotype with micropenis and blind vagina. The Tanner stage was A3B1P4, nonpalpable gonads. The karyotype revealed 46, XY. The endocrinology study revealed: testosterone = 2.38ng/ml, Delta 4> 10.00 ng/ml, and low testosterone/Delta 4 ratio = 0.23. Magnetic resonance imaging of the abdominal-pelvic showed the presence of testicles in inguinal canal, seminal vesicle, prostate, micropenis, and absence of uterus and vagina. The genetic study confirmed the mutation p.Glu215Asp on HSD17B3 gene in homozygosity. The dilemma of sex reassignment was seriously considered when the diagnosis was made. During all procedures the patient was accompanied by a child psychiatrist/psychologist. The teenager desired to continue being a female, so gonadectomy was performed. Estrogen therapy and surgical procedure to change external genitalia was carried out. In this case, there was a severe virilization at puberty. It is speculated to be due to a partial activity of 17bHSD3 in the testicles and/or extratesticular ability to convert D4 to testosterone by 17 beta HSD5. Prenatal exposure of the brain to androgens has increasingly been put forward as a critical factor in gender identity development, but in this case the social factor was more important for the gender assignment.
引用
收藏
页数:4
相关论文
共 26 条
  • [1] 46,XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency
    Mendonca, Berenice B.
    Gomes, Nathalia Lisboa
    Costa, Elaine M. F.
    Inacio, Marlene
    Martin, Regina M.
    Nishi, Mirian Y.
    Carvalho, Filomena Marino
    Tibor, Francisco Denes
    Domenice, Sorahia
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2017, 165 : 79 - 85
  • [2] 46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
    Galli-Tsinopoulou, Assimina
    Serbis, Anastasios
    Kotanidou, Eleni P.
    Litou, Eleni
    Dokousli, Vaia
    Mouzaki, Konstantina
    Fanis, Pavlos
    Neocleous, Vassos
    Skordis, Nicos
    JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2018, 10 (01) : 74 - 78
  • [3] 46, XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency: a plea for timely genetic testing
    Grimbly, Chelsey
    Caluseriu, Oana
    Metcalfe, Peter
    Jetha, Mary M.
    Rosolowsky, Elizabeth T.
    INTERNATIONAL JOURNAL OF PEDIATRIC ENDOCRINOLOGY, 2016,
  • [4] A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency
    Gurbuz, Fatih
    Turan, Ihsan
    Tastan, Mehmet
    Yuksel, Bilgin
    HORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 582 - 582
  • [5] Pubertal Development in 17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency
    Hiort, Olaf
    Marshall, Louise
    Birnbaum, Wiebke
    Wuensch, Lutz
    Holterhus, Paul-Martin
    Doehnert, Ulla
    Werner, Ralf
    HORMONE RESEARCH IN PAEDIATRICS, 2017, 87 (05): : 354 - 358
  • [6] 17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up
    Faienza, M. F.
    Baldinotti, F.
    Marrocco, G.
    TyuTyusheva, N.
    Peroni, D.
    Baroncelli, G. I.
    Bertelloni, S.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2020, 43 (12) : 1711 - 1716
  • [7] 17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-up
    M. F. Faienza
    F. Baldinotti
    G. Marrocco
    N. TyuTyusheva
    D. Peroni
    G. I. Baroncelli
    S. Bertelloni
    Journal of Endocrinological Investigation, 2020, 43 : 1711 - 1716
  • [8] Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients
    Goncalves, Catarina, I
    Carrico, Josianne
    Bastos, Margarida
    Lemos, Manuel C.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (17)
  • [9] 17-β-hydroxysteroid dehydrogenase type 3 deficiency as a rare cause of 46, XY Disorder of Sexual Development and Gender Dysphoria
    Jelley, Hannah
    Meder, Michelle
    Murray, Mary
    Schaeffer, Anthony
    Hayes, Katherine
    Daboub, Josue Flores
    Robnett, Jessica
    Rutz, Audrey
    Timme, Kathleen
    HORMONE RESEARCH IN PAEDIATRICS, 2021, 94 (SUPPL 2): : 114 - 115
  • [10] Rare Cause of 46,XY Sexual Development Disorder: 17β-Hydroxysteroid Dehydrogenase Type 3 Deficiency
    Manyas, Hayrullah
    Filibeli, Berna Eroglu
    Ayranci, Ilkay
    Guvenc, Merve Saka
    Dundar, Bumin Nuri
    Catli, Gonul
    HORMONE RESEARCH IN PAEDIATRICS, 2019, 91 : 600 - 600