Quality of life of patients with 46,XX and 46,XY disorders of sex development

被引:25
|
作者
Amaral, Rita Cassia [1 ]
Inacio, Marlene [1 ]
Brito, Vinicius N. [1 ]
Bachega, Tania A. S. S. [1 ]
Domenice, Sorahia [1 ]
Arnhold, Ivo J. P. [1 ]
Madureira, Guiomar [1 ]
Gomes, Larissa [1 ]
Costa, Elaine M. F. [1 ]
Mendonca, Berenice B. [1 ]
机构
[1] Univ Sao Paulo, Fac Med, Lab Hormonios & Genet Mol LIM 42,Hosp Clin, Unidade Endocrinol Desenvolvimento,Disciplina End, Sao Paulo, Brazil
关键词
CONGENITAL ADRENAL-HYPERPLASIA; 21-HYDROXYLASE DEFICIENCY; FEMALE-PATIENTS; WOMEN; HEALTH; ADULTS; INSTRUMENT; GENITALIA; VERSION;
D O I
10.1111/cen.12561
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Disorders of sex development (DSD) result from abnormalities in the complex process of sex determination and differentiation. An important consideration to guide the assignment of social sex in newborns with ambiguous genitalia is the quality of life (QoL) of these patients in adulthood. The rarity of most DSD conditions makes it difficult to conduct a long-term follow-up of affected patients through adulthood. This review of papers on the QoL of DSD patients evaluated in developing and developed countries by qualitative and quantitative instruments revealed a large spectrum of QoL, ranging from very poor to similar to, or even better than, the normal population. A more adequate QoL was found in patients from tertiary centres, indicating that the medical care of DSD patients should be multidisciplinary and carried out by specialized teams.
引用
收藏
页码:159 / 164
页数:6
相关论文
共 50 条
  • [31] Prostate screening in patients with 46,XY disorders of sex development - Is it necessary? Reply by authors
    不详
    JOURNAL OF UROLOGY, 2008, 180 (04): : 1426 - 1426
  • [32] Phenotype and genetic characteristics in 20 Chinese patients with 46,XY disorders of sex development
    Zheng, G. Y.
    Chu, G. M.
    Li, P. P.
    He, R.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2023, 46 (08) : 1613 - 1622
  • [33] Prostate screening in patients with 46,XY disorders of sex development - Is it necessary? Editorial comments
    Grubb, Robert L., III
    JOURNAL OF UROLOGY, 2008, 180 (04): : 1425 - 1425
  • [34] Phenotype and genetic characteristics in 20 Chinese patients with 46,XY disorders of sex development
    G. Y. Zheng
    G. M. Chu
    P. P. Li
    R. He
    Journal of Endocrinological Investigation, 2023, 46 : 1613 - 1622
  • [35] MOLECULAR AND CELLULAR CHARACTERIZATION OF PATIENTS WITH 46,XX TESTICULAR AND OVOTESTICULAR DISORDERS OF SEX DEVELOPMENT
    Touzon, Maria S.
    Berensztein, Esperanza
    Ramirez, Pablo
    Garrido, Natalia Perez
    Marino, Roxana
    Galluzzo, Laura
    Aliberti, Paula
    Costanzo, Mariana
    Guercio, Gabriela
    Vaiani, Elisa
    Ciaccio, Marta
    Rivarola, Marco A.
    Yatsenko, Svetlana A.
    Rajkovic, Aleksandar
    Belgorosky, Alicia
    HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 199 - 200
  • [36] 46,XY disorders of sex development: the use of NGS for prevalent variants
    Qi-Gen Xie
    Peng Luo
    Kai Xia
    Zuo-Qing Li
    Zhe Xu
    Cheng Su
    Chun-Hua Deng
    Human Genetics, 2022, 141 : 1863 - 1873
  • [37] Disorders/Differences of Sex Development Presenting in the Newborn With 46,XY Karyotype
    Bertelloni, Silvano
    Tyutyusheva, Nina
    Valiani, Margherita
    D'Alberton, Franco
    Baldinotti, Fulvia
    Caligo, Maria Adelaide
    Baroncelli, Giampiero I.
    Peroni, Diego G.
    FRONTIERS IN PEDIATRICS, 2021, 9
  • [38] Behavioural Problems in Children with 46XY Disorders of Sex Development
    Selveindran, Nalini M.
    Zakaria, Syed Zulkifli Syed
    Jalaludin, Muhammad Yazid
    Rasat, Rahmah
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2017, 2017
  • [39] Etiological structure disorders of sex development 46, xy by one center
    Sannikova, Ekate
    Samsonova, Lubov
    Latyshev, Oleg
    Kiseleva, Elena
    Okminyan, Goar
    Kasatkina, Elvira
    Dondup, Olga
    Okulov, Alexey
    Tulpakov, Anatoliy
    HORMONE RESEARCH IN PAEDIATRICS, 2019, 91 : 475 - 475
  • [40] 46,XY disorders of sex development: the use of NGS for prevalent variants
    Xie, Qi-Gen
    Luo, Peng
    Xia, Kai
    Li, Zuo-Qing
    Xu, Zhe
    Su, Cheng
    Deng, Chun-Hua
    HUMAN GENETICS, 2022, 141 (12) : 1863 - 1873