Detection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastoma.

J Pediatr Endocrinol Metab

Division of Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, Brazil.

Published: September 2006

Unlabelled: The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase the risk of gonadoblastoma. The investigation of Y sequences is usually performed only in the presence of marker chromosomes and therefore does not rule out the presence of hidden mosaicism in patients with 45,X TS without any marker.

Aims: 1. To investigate the presence of hidden Y mosaicism in non-mosaic 45,X patients with TS, using samples from different tissues, and its association with the development of gonadoblastoma.

Study Design: Twenty patients with a 45,X karyotype were studied. The SRY and DYZ3 sequences were amplified by PCR, using genomic DNA from peripheral blood, oral epithelial cells and hair roots. Prophylactic gonadectomy was offered to the Y-positive patients.

Results: The analysis of the different tissues revealed that seven (35%) out of the 20 patients studied presented hidden chromosome Y mosaicism. Four of these patients underwent prophylactic gonadectomy, and bilateral gonadoblastoma was found in one of them.

Conclusions: A systematic search for hidden Y chromosome mosaicism in patients with TS and 45,X karyotype is justified by the possibility of developing gonadoblastoma.

Download full-text PDF

Source
http://dx.doi.org/10.1515/jpem.2006.19.9.1113DOI Listing

Publication Analysis

Top Keywords

hidden mosaicism
12
mosaicism patients
12
patients 45x
12
turner's syndrome
8
presence hidden
8
45x karyotype
8
prophylactic gonadectomy
8
hidden chromosome
8
chromosome mosaicism
8
patients
7

Similar Publications

A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities.

Genome Res

November 2024

Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, 171 77 Stockholm, Sweden;

Clinical genetic laboratories often require a comprehensive analysis of chromosomal rearrangements/structural variants (SVs), from large events like translocations and inversions to supernumerary ring/marker chromosomes and small deletions or duplications. Understanding the complexity of these events and their clinical consequences requires pinpointing breakpoint junctions and resolving the derivative chromosome structure. This task often surpasses the capabilities of short-read sequencing technologies.

View Article and Find Full Text PDF
Article Synopsis
  • Tuberous sclerosis, a genetic disorder caused by mutations in TSC1 or TSC2, often leaves some patients with no identifiable mutation.
  • Researchers sequenced DNA from 26 such patients, hypothesizing that structural or deep intronic variants might be responsible.
  • They discovered likely pathogenic variants in 13 patients, including large deletions and complex rearrangements, indicating potential new types of mutations and suggesting long-read sequencing is effective for diagnosing cases previously categorized as "no mutation identified."
View Article and Find Full Text PDF

Environmental viruses (primarily bacteriophages) are widely recognized as playing an important role in ecosystem homeostasis through the infection of host cells. However, the majority of environmental viruses are still unknown as their mosaic structure and frequent mutations in their sequences hinder genome construction in current metagenomics. To enable the large-scale acquisition of environmental viral genomes, we developed a new single-viral genome sequencing platform with microfluidic-generated gel beads.

View Article and Find Full Text PDF

Exploring undiscovered public knowledge in neuroscience.

Eur J Neurosci

September 2024

Departamento de Psicobiologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.

In this essay, I argue that the combination of research synthesis and philosophical methods can fill an important methodological gap in neuroscience. While experimental research and formal modelling have seen their methods progressively increase in rigour and sophistication over the years, the task of analysing and synthesizing the vast literature reporting new results and models has lagged behind. The problem is aggravated because neuroscience has grown and expanded into a vast mosaic of related but partially independent subfields, each with their own literatures.

View Article and Find Full Text PDF

Background: Girls with Turner syndrome (TS) lack a partial or complete sex chromosome, which causes an accelerated decline of their ovarian reserve. Girls have to deal with several dilemmas related to their fertility, while only a limited number of them are referred to a fertility specialist and counselled about options of family planning on time.

Objective And Rationale: This scoping review provides an update of the literature on fertility in girls with TS throughout their lifespan and aims to propose a clinical practice guideline on fertility in TS.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!