Turner Syndrome with Y Chromosome and Germ Cells: A Case Report Highlighting the Need to Prioritize Individualized Care.
Journal
Urology
ISSN: 1527-9995
Titre abrégé: Urology
Pays: United States
ID NLM: 0366151
Informations de publication
Date de publication:
31 May 2024
31 May 2024
Historique:
received:
07
05
2024
accepted:
20
05
2024
medline:
3
6
2024
pubmed:
3
6
2024
entrez:
2
6
2024
Statut:
aheadofprint
Résumé
Turner syndrome (TS) is a genetic condition in phenotypic females in which the individual has one intact X chromosome and the second sex chromosome is absent or structurally alteredComponents of Y chromosome (e.g., 45,X/46,XY) have been found in 5-15% of patients with TS; these patients are often referred to as having "Turner syndrome with Y" (TS+Y). The presence of Y chromosome material increases risk for development of gonadal tumors. Historically, prophylactic gonadectomy has been recommended in this population to prevent malignancy, and patients were presumed infertile due to the presence of streak gonads with no germ cells (GCs). More recently, studies have reported on spontaneous puberty and menarche in TS+Y patients suggesting the presence of viable GC and ovarian function. Our institution offers patients with TS+Y the option of experimental gonadal tissue cryopreservation (GTC) at the time of gonadectomy. We present a unique case of a young girl with TS+Y who had GCs present in her gonads and underwent experimental GTC at the time of gonadectomy.
Identifiants
pubmed: 38825087
pii: S0090-4295(24)00412-6
doi: 10.1016/j.urology.2024.05.020
pii:
doi:
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest All authors have indicated they have no potential conflicts of interest or financial relationships relevant to the article to disclose.