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A patient with 46,XY/47,XYY karyotype and female phenotype: a case report

A patient with 46,XY/47,XYY karyotype and female phenotype: a case report

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7fe60b9d2ac449689e2e32fd7db5e7b1

A patient with 46,XY/47,XYY karyotype and female phenotype: a case report

About this item

Full title

A patient with 46,XY/47,XYY karyotype and female phenotype: a case report

Publisher

England: BioMed Central Ltd

Journal title

BMC endocrine disorders, 2020-03, Vol.20 (1), p.42-42, Article 42

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

47,XYY is a chromosomal abnormality syndrome that is typically observed in patients with a male phenotype. Few patients with XYY syndrome will have infertility. We here report a case of 46,XY/47,XYY syndrome diagnosed in a patient with a female phenotype.
A 15-year-old patient with a female phenotype visited our hospital owing to a chief complai...

Alternative Titles

Full title

A patient with 46,XY/47,XYY karyotype and female phenotype: a case report

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_7fe60b9d2ac449689e2e32fd7db5e7b1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7fe60b9d2ac449689e2e32fd7db5e7b1

Other Identifiers

ISSN

1472-6823

E-ISSN

1472-6823

DOI

10.1186/s12902-020-0523-8

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