Ring Y chromosome as an unusual cause of severe oligozoospermia

RCY is a rare but important genetic cause of male infertility and should be considered in the evaluation of severe oligozoospermia or azoospermia. The clinical phenotype of RCY ranges from a normal male phenotype with infertility to phenotypic females with features of Turner syndrome. This is influenced by the presence or absence of Y-linked genes and the degree of 45,X mosaicism. The presence of a 45,X cell line in individuals with RCY mosaicism has been associated with gonadal anomalies, particularly dysgenesis and cryptorchidism.

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Publication Details

Journal
Endocrinology Diabetes and Metabolism Case Reports
Published
2025-10-01
DOI
https://doi.org/10.1530/edm-25-0113
Citations
1
Primary Topic
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Type
article
Field-Weighted Citation Impact
1.82
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article

Ring Y chromosome as an unusual cause of severe oligozoospermia

Christopher A. Muir, Serena Chong
1 citations
Endocrinology Diabetes and Metabolism Case Reports
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
1.82
article

Ring Y chromosome as an unusual cause of severe oligozoospermia

Christopher A. Muir, Serena Chong
article en
1 citations

Abstract

RCY is a rare but important genetic cause of male infertility and should be considered in the evaluation of severe oligozoospermia or azoospermia. The clinical phenotype of RCY ranges from a normal male phenotype with infertility to phenotypic females with features of Turner syndrome. This is influenced by the presence or absence of Y-linked genes and the degree of 45,X mosaicism. The presence of a 45,X cell line in individuals with RCY mosaicism has been associated with gonadal anomalies, particularly dysgenesis and cryptorchidism.

Endocrinology Diabetes and Metabolism Case ReportsVol. 2025(4)
Concord Repatriation General Hospital (AU), UNSW Sydney (AU), St Vincent's Hospital Sydney (AU)
Openalex Percentile: Top 11%
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
1.82
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