45,X[2]/46,X,der(Y).ish Psu idic(Y)(q11.2)[38] mosaic karyotype in mixed gonadal dysgenesis: a case report and literature review
Mixed gonadal dysgenesis is caused by a variety of chromosome abnormalities, most commonly Y chromosome mosaicism. An 8-year-old boy presented with short stature for possible treatment with recombinant growth hormone. He had a history of mixed gonadal dysgenesis (hypospadias, bilateral cryptorchidism, processus vaginalis, and dysplastic immature uterus) and a series of corrective surgeries. At 14 months of age, chromosomal karyotyping revealed 46,X,+mar. Upon presentation, lab testing was consistent with the male phenotype at prepuberty. Fluorescence <i>in situ</i> hybridization revealed 45,X[2]/46,X,der(Y).ish psu idic(Y)(q11.2)(SRY++,DYZ3++)[38] karyotype. A literature review identified eight case reports of mixed gonadal dysgenesis associated with 45,X/46,X,idic(Y)(q11.2). Neither sex phenotype nor short stature correlated with the 46,X,idic(Y)(q11.2) mosaic ratio.
Authors
- Yang Liu (ORCID: https://orcid.org/0000-0003-3175-8490)
- Yun Zhou (ORCID: https://orcid.org/0000-0001-6179-5407)
- Xiaowei Cui (ORCID: https://orcid.org/0000-0002-9325-3765)
- Lei Liu (ORCID: https://orcid.org/0000-0002-0839-0678)
- Lijun Liu (ORCID: https://orcid.org/0000-0002-2835-7082)
- Qiang Zhang (ORCID: https://orcid.org/0000-0002-2707-0258)
- Xiaoxiao Chen (ORCID: https://orcid.org/0000-0003-3907-8465)
- Yanyan Cao (ORCID: https://orcid.org/0000-0002-6407-9446)
Institutions
- Hospital of Hebei Province (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2024-10-16
- DOI
- https://doi.org/10.3389/fped.2024.1460174
- Primary Topic
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00