Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series.

doi:10.1111/and.13009

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series.

Andrologia - 1 Jun 2018

Mohammadpour Lashkari F, Sadighi Gilani M A, Ghaheri A, Zamanian M R, Borjian Boroujeni P, Mohseni Meybodi A, Sabbaghian M

Abstract excerpt

Disorders of sex development (DSD) are congenital abnormalities as an atypical development process in either gonadal or chromosomal structure. It is the cause of the abnormality in phenotype and characteristics. Chromosomal analysis plays an important role in the DSD determination. 45,X/46,XY mosaicism is a rare karyotype, and its prevalence is about 1.5 in 10,000 newborns. It affects the growth, hormonal...

Topics

Adult
Follicle Stimulating Hormone
Humans
Infertility, Male
Karyotyping
Luteinizing Hormone
Male
Mosaicism
Organ Size
Phenotype
Reproductive Techniques, Assisted
Sex Chromosome Aberrations
Testis
Testosterone

Source

Open in PubMed

Identifiers

PMID: 29527714
DOI: 10.1111/and.13009

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics